NO143939B - Alfa-(4-(4`-trifluormetylfenoksy)-fenoksy)-propionsyrer og derivater herav for anvendelse som herbicider - Google Patents

Alfa-(4-(4`-trifluormetylfenoksy)-fenoksy)-propionsyrer og derivater herav for anvendelse som herbicider Download PDF

Info

Publication number: NO143939B
Authority: NO; Norway
Prior art keywords: phenoxy; acid; derivatives; weeds; trifluoromethyl
Prior art date: 1974-07-10

Application number

NO752466A

Other languages

English (en)

Norwegian (no)

Other versions

NO752466L (fr

Inventor

Juergen Troesken

Gerhard Hoerlein

Ernst-Friedrich Schulze

Langelueddeke

Brd

Original Assignee

Hoechst Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1974-07-10

Filing date

1975-07-09

Publication date

1981-02-02

1975-07-09 Application filed by Hoechst Ag filed Critical Hoechst Ag

1976-01-13 Publication of NO752466L publication Critical patent/NO752466L/no

1981-02-02 Publication of NO143939B publication Critical patent/NO143939B/no

Links

-1 4- (4`-TRIFLUORMETHYLPHENOXY) -PHENOXY Chemical class 0.000 title claims description 11
239000004009 herbicide Substances 0.000 title claims description 11
241000196324 Embryophyta Species 0.000 claims description 48
150000001875 compounds Chemical class 0.000 claims description 21
229910052736 halogen Inorganic materials 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 6
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
239000001257 hydrogen Substances 0.000 claims description 5
229910052739 hydrogen Inorganic materials 0.000 claims description 5
125000003282 alkyl amino group Chemical group 0.000 claims description 4
150000001768 cations Chemical class 0.000 claims description 4
150000007530 organic bases Chemical class 0.000 claims description 4
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
150000007529 inorganic bases Chemical class 0.000 claims description 2
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
125000005843 halogen group Chemical group 0.000 claims 1
239000000126 substance Substances 0.000 description 35
239000013543 active substance Substances 0.000 description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
239000002253 acid Substances 0.000 description 15
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 14
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
239000000203 mixture Substances 0.000 description 10
244000075850 Avena orientalis Species 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Substances CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 8
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244000062793 Sorghum vulgare Species 0.000 description 7
235000019713 millet Nutrition 0.000 description 7
239000011734 sodium Substances 0.000 description 7
229910052708 sodium Inorganic materials 0.000 description 7
239000002689 soil Substances 0.000 description 7
239000000243 solution Substances 0.000 description 7
MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 description 6
240000001592 Amaranthus caudatus Species 0.000 description 6
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
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MWBPRDONLNQCFV-UHFFFAOYSA-N Tri-allate Chemical compound CC(C)N(C(C)C)C(=O)SCC(Cl)=C(Cl)Cl MWBPRDONLNQCFV-UHFFFAOYSA-N 0.000 description 6
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000008187 granular material Substances 0.000 description 6
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244000052363 Cynodon dactylon Species 0.000 description 5
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235000011301 Brassica oleracea var capitata Nutrition 0.000 description 4
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235000021536 Sugar beet Nutrition 0.000 description 4
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239000000080 wetting agent Substances 0.000 description 3
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244000025254 Cannabis sativa Species 0.000 description 2
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QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
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240000004713 Pisum sativum Species 0.000 description 2
235000010582 Pisum sativum Nutrition 0.000 description 2
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WOZQBERUBLYCEG-UHFFFAOYSA-N SWEP Chemical compound COC(=O)NC1=CC=C(Cl)C(Cl)=C1 WOZQBERUBLYCEG-UHFFFAOYSA-N 0.000 description 1
235000005775 Setaria Nutrition 0.000 description 1
241000232088 Setaria <nematode> Species 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
XJCLWVXTCRQIDI-UHFFFAOYSA-N Sulfallate Chemical compound CCN(CC)C(=S)SCC(Cl)=C XJCLWVXTCRQIDI-UHFFFAOYSA-N 0.000 description 1
SAQSTQBVENFSKT-UHFFFAOYSA-M TCA-sodium Chemical compound [Na+].[O-]C(=O)C(Cl)(Cl)Cl SAQSTQBVENFSKT-UHFFFAOYSA-M 0.000 description 1
WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 description 1
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235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
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239000000654 additive Substances 0.000 description 1
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239000003513 alkali Substances 0.000 description 1
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RQVYBGPQFYCBGX-UHFFFAOYSA-N ametryn Chemical compound CCNC1=NC(NC(C)C)=NC(SC)=N1 RQVYBGPQFYCBGX-UHFFFAOYSA-N 0.000 description 1
230000009435 amidation Effects 0.000 description 1
238000007112 amidation reaction Methods 0.000 description 1
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150000001448 anilines Chemical class 0.000 description 1
239000008346 aqueous phase Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
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MCOQHIWZJUDQIC-UHFFFAOYSA-N barban Chemical compound ClCC#CCOC(=O)NC1=CC=CC(Cl)=C1 MCOQHIWZJUDQIC-UHFFFAOYSA-N 0.000 description 1
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229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
229940092714 benzenesulfonic acid Drugs 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
WYKYKTKDBLFHCY-UHFFFAOYSA-N chloridazon Chemical class O=C1C(Cl)=C(N)C=NN1C1=CC=CC=C1 WYKYKTKDBLFHCY-UHFFFAOYSA-N 0.000 description 1
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239000004927 clay Substances 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
229960001760 dimethyl sulfoxide Drugs 0.000 description 1
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 1
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238000010410 dusting Methods 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
230000008029 eradication Effects 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
ARFLASKVLJTEJD-UHFFFAOYSA-N ethyl 2-bromopropanoate Chemical compound CCOC(=O)C(C)Br ARFLASKVLJTEJD-UHFFFAOYSA-N 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
RZILCCPWPBTYDO-UHFFFAOYSA-N fluometuron Chemical compound CN(C)C(=O)NC1=CC=CC(C(F)(F)F)=C1 RZILCCPWPBTYDO-UHFFFAOYSA-N 0.000 description 1
238000005755 formation reaction Methods 0.000 description 1
238000005469 granulation Methods 0.000 description 1
230000003179 granulation Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
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239000002917 insecticide Substances 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
NRXQIUSYPAHGNM-UHFFFAOYSA-N ioxynil Chemical compound OC1=C(I)C=C(C#N)C=C1I NRXQIUSYPAHGNM-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000004310 lactic acid Substances 0.000 description 1
235000014655 lactic acid Nutrition 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
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150000007517 lewis acids Chemical class 0.000 description 1
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235000009973 maize Nutrition 0.000 description 1
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JITOKQVGRJSHHA-UHFFFAOYSA-M monosodium methyl arsenate Chemical compound [Na+].C[As](O)([O-])=O JITOKQVGRJSHHA-UHFFFAOYSA-M 0.000 description 1
229940084719 monosodium methylarsonate Drugs 0.000 description 1
239000006199 nebulizer Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
230000002085 persistent effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
IDOWTHOLJBTAFI-UHFFFAOYSA-N phenmedipham Chemical compound COC(=O)NC1=CC=CC(OC(=O)NC=2C=C(C)C=CC=2)=C1 IDOWTHOLJBTAFI-UHFFFAOYSA-N 0.000 description 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
239000003880 polar aprotic solvent Substances 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000004540 pour-on Substances 0.000 description 1
AAEVYOVXGOFMJO-UHFFFAOYSA-N prometryn Chemical compound CSC1=NC(NC(C)C)=NC(NC(C)C)=N1 AAEVYOVXGOFMJO-UHFFFAOYSA-N 0.000 description 1
HHFOOWPWAXNJNY-UHFFFAOYSA-N promoxolane Chemical compound CC(C)C1(C(C)C)OCC(CO)O1 HHFOOWPWAXNJNY-UHFFFAOYSA-N 0.000 description 1
229950008352 promoxolane Drugs 0.000 description 1
MFOUDYKPLGXPGO-UHFFFAOYSA-N propachlor Chemical compound ClCC(=O)N(C(C)C)C1=CC=CC=C1 MFOUDYKPLGXPGO-UHFFFAOYSA-N 0.000 description 1
RZWZRACFZGVKFM-UHFFFAOYSA-N propanoyl chloride Chemical compound CCC(Cl)=O RZWZRACFZGVKFM-UHFFFAOYSA-N 0.000 description 1
239000003380 propellant Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
229910052903 pyrophyllite Inorganic materials 0.000 description 1
239000010453 quartz Substances 0.000 description 1
238000010992 reflux Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000007127 saponification reaction Methods 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
238000009331 sowing Methods 0.000 description 1
238000005507 spraying Methods 0.000 description 1
235000000346 sugar Nutrition 0.000 description 1
150000003459 sulfonic acid esters Chemical class 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
125000005490 tosylate group Chemical group 0.000 description 1
238000005809 transesterification reaction Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
229940066528 trichloroacetate Drugs 0.000 description 1
ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
- C07C59/66—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
- C07C59/68—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Hydrogenated Pyridines (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

NO752466A 1974-07-10 1975-07-09 Alfa-(4-(4`-trifluormetylfenoksy)-fenoksy)-propionsyrer og derivater herav for anvendelse som herbicider NO143939B (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19742433067 DE2433067B2 (de)	1974-07-10	1974-07-10	Alpha- eckige klammer auf 4-(4' trifluormethylphenoxy)-phenoxy eckige klammer zu -propionsaeuren und deren derivate, verfahren zu ihrer herstellung und diese enthaltende herbizide mittel

Publications (2)

Publication Number	Publication Date
NO752466L NO752466L (fr)	1976-01-13
NO143939B true NO143939B (no)	1981-02-02

Family

ID=5920140

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO752466A NO143939B (no)	1974-07-10	1975-07-09	Alfa-(4-(4`-trifluormetylfenoksy)-fenoksy)-propionsyrer og derivater herav for anvendelse som herbicider

Country Status (34)

Country	Link
US (1)	US4332960A (fr)
JP (1)	JPS6035321B2 (fr)
AR (1)	AR219048A1 (fr)
AT (1)	AT348288B (fr)
BE (1)	BE831218A (fr)
BG (1)	BG24937A3 (fr)
BR (1)	BR7504296A (fr)
CA (1)	CA1150294A (fr)
CH (1)	CH614601A5 (fr)
CS (1)	CS186289B2 (fr)
CU (1)	CU34303A (fr)
DD (1)	DD121592A5 (fr)
DE (1)	DE2433067B2 (fr)
DK (1)	DK310575A (fr)
EG (1)	EG11750A (fr)
ES (1)	ES439172A1 (fr)
FR (1)	FR2277811A1 (fr)
GB (1)	GB1519334A (fr)
HU (1)	HU176531B (fr)
IE (1)	IE42046B1 (fr)
IL (1)	IL47640A (fr)
IT (1)	IT1039818B (fr)
LU (1)	LU72924A1 (fr)
MW (1)	MW4075A1 (fr)
NL (1)	NL7508016A (fr)
NO (1)	NO143939B (fr)
OA (1)	OA05056A (fr)
RO (1)	RO68991A (fr)
SE (2)	SE7507833L (fr)
SU (1)	SU578856A3 (fr)
TR (1)	TR18262A (fr)
YU (1)	YU174375A (fr)
ZA (1)	ZA754053B (fr)
ZM (1)	ZM8575A1 (fr)

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FR2446812A1 (fr) *	1979-01-16	1980-08-14	Produits Ind Cie Fse	Phenoxy- et thiophenoxynitriles et leurs applications en tant qu'herbicides
DK220582A (da) *	1981-05-26	1982-11-27	Hoffmann La Roche	Propionsyreamider
JPS5832890A (ja) *	1981-08-21	1983-02-25	Sumitomo Chem Co Ltd	ホスホン酸エステル誘導体、その製造方法およびそれを有効成分とする除草剤
US4447259A (en) *	1981-12-18	1984-05-08	Hokko Chemical Industry Co., Ltd.	2-(Substituted phenoxy)propionic acid derivatives and their uses for herbicidal purposes
US4460399A (en) *	1982-01-26	1984-07-17	Chevron Research Company	Diphenoxy ether formamide plant-growth regulator
US4808750A (en) *	1983-09-01	1989-02-28	The Dow Chemical Company	Fluorophenoxyphenoxypropionates and derivatives thereof
US4550192A (en) *	1983-09-01	1985-10-29	The Dow Chemical Company	Fluorophenoxyphenoxypropionates and derivatives thereof
US4888050A (en) *	1983-11-10	1989-12-19	The Dow Chemical Company	Fluorophenoxy compounds, herbicidal compositions and methods
EP0305593A3 (fr) *	1983-12-06	1989-10-11	Ciba-Geigy Ag	Intermédiaires pour des cyanamides de l'acide pyridinyl-2-oxyphénoxypropionique
CN1008820B (zh) *	1985-05-10	1990-07-18	施林工业产权保护股份公司	17α-乙炔基-17β-羟基-18-甲基-4，15-雌甾二烯-3-酮的制备方法
US4589907A (en) *	1985-09-17	1986-05-20	Stauffer Chemical Company	Amidomethyl ester herbicides
JPS638861A (ja) *	1986-06-27	1988-01-14	Anritsu Corp	磁気カードとその識別装置
US4786731A (en) *	1987-08-05	1988-11-22	The Dow Chemical Company	Resolution of enantiomers of 2-(phenyl or phenoxy/propionic acids using optically active alkanolamines
US4786732A (en) *	1987-08-05	1988-11-22	The Dow Chemical Company	Resolution of enantiomers of 2-(4-aryloxyphenoxy) propionic acids by liquid chromatography with a chiral eluent
US4897481A (en) *	1988-05-31	1990-01-30	The Dow Chemical Company	Process for the minimization of racemization in the preparation of optically active ((aryloxy)phenoxy)propionate herbicides
US5012017A (en) *	1988-08-18	1991-04-30	Dowelanco	Phenoxyphenoxypropionates, intermediates thereof and methods of preparation
DE3902439A1 (de) *	1989-01-27	1990-08-02	Basf Ag	Pflanzenschuetzende mittel auf basis von 1-aryl- bzw. 1-hetarylimidazolcarbonsaeureestern
DE3907938A1 (de) *	1989-03-11	1990-09-13	Basf Ag	2,3-substituierte 1,8-naphthyridine, verfahren zu ihrer herstellung und ihre verwendung als antidots
DE4318092C1 (de) *	1993-06-01	1995-01-12	Basf Ag	Verfahren zur Herstellung von (R)- oder (S)-2-(4-Alkanoylphenoxy)- und (R)- oder (S)-2-(4-Aroylphenoxy)-propionsäureestern
EP1836894A1 (fr)	2006-03-25	2007-09-26	Bayer CropScience GmbH	Nouvelles formulations solides à base de sulfonamides
DE102007013362A1 (de)	2007-03-16	2008-09-18	Bayer Cropscience Ag	Penetrationsförderer für herbizide Wirkstoffe
EP1844654A1 (fr)	2006-03-29	2007-10-17	Bayer CropScience GmbH	Activateur de la pénétration foliaire des principes actives agrochimiques
WO2011076731A1 (fr)	2009-12-23	2011-06-30	Bayer Cropscience Ag	Formulation liquide de 2-iodo-n-[(4-méthoxy-6-méthyl-1, 3, 5-triazin-2-yl) carbamoyl] benzène sulfonamide
CA2827159A1 (fr)	2011-02-15	2012-08-23	Ruth Meissner	Combinaisons synergiques contenant un fongicide dithiino-tetracarboxamide et un herbicide, un phytoprotecteur ou un regulateur de croissance vegetale
DE102011080020A1 (de)	2011-07-28	2012-09-13	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Dicarboximid-Fungizide als Safener
DE102011080001A1 (de)	2011-07-28	2012-10-25	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Carbamat-Insektizide als Safener
DE102011080010A1 (de)	2011-07-28	2012-10-25	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Anilid- und Thiazol-Fungizide als Safener
DE102011080007A1 (de)	2011-07-28	2012-09-13	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus den Gruppen der Conazole- und Triazol-Fungizide als Safener
DE102011080016A1 (de)	2011-07-28	2012-10-25	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Strobilurin-Fungizide als Safener
DE102011079991A1 (de)	2011-07-28	2012-09-13	Bayer Crop Science Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Nicotinoid-Insektizide als Safener
DE102011080004A1 (de)	2011-07-28	2012-09-13	Bayer Cropscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Carbamat-Fungizide als Safener
DE102011079997A1 (de)	2011-07-28	2012-09-13	Bayer Corpscience Ag	Verwendung von Saatgutbehandlungs-Wirkstoffen aus der Gruppe der Pyrazol-Insektizide als Safener
JP6153619B2 (ja)	2012-10-19	2017-06-28	バイエル・クロップサイエンス・アクチェンゲゼルシャフト	カルボキサミド誘導体を含む活性化合物の組み合わせ

1974
- 1974-07-10 DE DE19742433067 patent/DE2433067B2/de active Granted
1975
- 1975-06-25 ZA ZA00754053A patent/ZA754053B/xx unknown
- 1975-06-25 EG EG75360A patent/EG11750A/xx active
- 1975-07-01 RO RO7582720A patent/RO68991A/fr unknown
- 1975-07-03 IL IL47640A patent/IL47640A/xx unknown
- 1975-07-03 SU SU7502149601A patent/SU578856A3/ru active
- 1975-07-04 TR TR18262A patent/TR18262A/xx unknown
- 1975-07-04 ES ES439172A patent/ES439172A1/es not_active Expired
- 1975-07-04 NL NL7508016A patent/NL7508016A/xx not_active Application Discontinuation
- 1975-07-05 BG BG7500030473A patent/BG24937A3/xx unknown
- 1975-07-07 AT AT520275A patent/AT348288B/de not_active IP Right Cessation
- 1975-07-07 CH CH884475A patent/CH614601A5/xx not_active IP Right Cessation
- 1975-07-08 US US05/594,031 patent/US4332960A/en not_active Expired - Lifetime
- 1975-07-08 MW MW40/75A patent/MW4075A1/xx unknown
- 1975-07-08 GB GB28690/75A patent/GB1519334A/en not_active Expired
- 1975-07-08 DD DD187159A patent/DD121592A5/xx unknown
- 1975-07-08 BR BR5508/75D patent/BR7504296A/pt unknown
- 1975-07-08 IT IT25205/75A patent/IT1039818B/it active
- 1975-07-08 LU LU72924A patent/LU72924A1/xx unknown
- 1975-07-08 SE SE7507833A patent/SE7507833L/xx unknown
- 1975-07-09 IE IE1528/75A patent/IE42046B1/en unknown
- 1975-07-09 FR FR7521511A patent/FR2277811A1/fr active Granted
- 1975-07-09 NO NO752466A patent/NO143939B/no unknown
- 1975-07-09 HU HU75HO1818A patent/HU176531B/hu unknown
- 1975-07-09 YU YU01743/75A patent/YU174375A/xx unknown
- 1975-07-09 CA CA000231130A patent/CA1150294A/fr not_active Expired
- 1975-07-09 ZM ZM85/75A patent/ZM8575A1/xx unknown
- 1975-07-09 DK DK310575A patent/DK310575A/da not_active Application Discontinuation
- 1975-07-09 JP JP50083632A patent/JPS6035321B2/ja not_active Expired
- 1975-07-10 CS CS7500004917A patent/CS186289B2/cs unknown
- 1975-07-10 AR AR259508A patent/AR219048A1/es active
- 1975-07-10 OA OA55556A patent/OA05056A/fr unknown
- 1975-07-10 BE BE158168A patent/BE831218A/fr unknown
- 1975-07-12 CU CU34303A patent/CU34303A/es unknown
1978
- 1978-01-27 SE SE7801047A patent/SE7801047L/xx unknown

Also Published As

Publication number	Publication date
JPS5132730A (en)	1976-03-19
CU34303A (es)	1983-10-04
AR219048A1 (es)	1980-07-31
CA1150294A (fr)	1983-07-19
IL47640A (en)	1978-01-31
OA05056A (fr)	1980-12-31
JPS6035321B2 (ja)	1985-08-14
BG24937A3 (en)	1978-06-15
EG11750A (en)	1978-12-31
FR2277811B1 (fr)	1978-10-27
DK310575A (da)	1976-01-11
HU176531B (en)	1981-03-28
BR7504296A (pt)	1976-07-06
SE7507833L (sv)	1976-01-12
ES439172A1 (es)	1977-06-16
IE42046B1 (en)	1980-05-21
DE2433067A1 (de)	1976-01-29
CH614601A5 (fr)	1979-12-14
CS186289B2 (en)	1978-11-30
NO752466L (fr)	1976-01-13
BE831218A (fr)	1976-01-12
FR2277811A1 (fr)	1976-02-06
CU21021L (en)	1979-01-16
US4332960A (en)	1982-06-01
IL47640A0 (en)	1975-10-15
NL7508016A (nl)	1976-01-13
AU8286975A (en)	1977-01-13
GB1519334A (en)	1978-07-26
ZM8575A1 (en)	1976-03-22
IT1039818B (it)	1979-12-10
SE7801047L (sv)	1978-01-27
IE42046L (en)	1976-01-10
ZA754053B (en)	1976-06-30
DD121592A5 (fr)	1976-08-12
TR18262A (tr)	1976-11-10
LU72924A1 (fr)	1977-03-24
ATA520275A (de)	1978-06-15
YU174375A (en)	1983-01-21
RO68991A (fr)	1981-06-26
DE2433067B2 (de)	1977-11-24
AT348288B (de)	1979-02-12
DE2433067C3 (fr)	1978-07-13
MW4075A1 (en)	1976-12-08
SU578856A3 (ru)	1977-10-30

Publication	Publication Date	Title
NO143939B (no)	1981-02-02	Alfa-(4-(4`-trifluormetylfenoksy)-fenoksy)-propionsyrer og derivater herav for anvendelse som herbicider
JP6258174B2 (ja)	2018-01-10	除草性カルボン酸及び水酸化テトラアルキルアンモニウム又は水酸化（アリールアルキル）トリアルキルアンモニウムから誘導される化合物
NO751243L (fr)	1975-10-13
WO1999045774A1 (fr)	1999-09-16	Agent regulant la croissance de vegetaux
EP0288275B1 (fr)	1993-01-27	Dérivés d'acide phénoxypropionique utiles comme herbicides
JPS61229876A (ja)	1986-10-14	新規なアニリノベンゾオキソール化合物、その製造方法、及び該化合物を含有する組成物、並びに前記化合物の使用方法
US3637720A (en)	1972-01-25	Certain substituted pyridyl phenyl ethers
CS198300B2 (en)	1980-05-30	Herbicide and method of producing the active ingredient
CN115701430A (zh)	2023-02-10	一种含异恶唑啉的苯基吡啶类化合物及其用途
US4945113A (en)	1990-07-31	herbicidal sulfonamide derivatives
JPS62169764A (ja)	1987-07-25	１、２−ジ置換ピペリンジン、それらの製造方法および植物保護におけるそれらの用途
US4692185A (en)	1987-09-08	N-(ortho-substituted) benzyl, 3-trifluoromethylphenoxy nicotinamides as herbicides
JPS5838422B2 (ja)	1983-08-23	置換シクロプロピルメトキシアニライド及び除草組成物
JPS61229890A (ja)	1986-10-14	リン含有官能性酢酸誘導体、その製造方法およびそれらを含有する除草剤および植物生長調整剤
JPH02264770A (ja)	1990-10-29	植物を病気から保護するための組成物
JPS58183666A (ja)	1983-10-26	置換フエノキシプロピオン酸エステル、その製造中間体、該エステル及び該中間体の製法、並びに除草剤
EP0098440B1 (fr)	1986-12-30	Dérivés de la 3,7-dichloroquinoléine, procédé pour leur préparation et leur utilisation pour lutter contre la croissance non-désirable des plantes
US4509974A (en)	1985-04-09	S-n-Butyl-N,N-diisopropyl thiocarbamate as a selective herbicide in cotton
NL8903166A (nl)	1990-07-16	Nieuw herbicidepreparaat.
KR820001713B1 (ko)	1982-09-21	α-[4-(4'-트리폴루오르메틸페녹시)-페녹시]알칸카르복시산 유도체의 제조방법
HU189919B (en)	1986-08-28	Herbicide containing new 2-methyl-4-isopropyl-2-pentenoil-anilide compounds as agent and process for the production of the agent
DD208068A5 (de)	1984-03-28	Herbizidzusammensetzung und verfahren zur vernichtung unerwuenschter pflanzen
CA1196644A (fr)	1985-11-12	Esters d'acide phenoxypropionique substitues et produits intermediaires; methode de preparation et utilisation comme herbicide
KR820000804B1 (ko)	1982-05-11	페녹시-페녹시 프로피온산 유도체의 제조방법
US4692186A (en)	1987-09-08	S-n-butyl-N,N-diisopropyl thiocarbamate as a selective herbicide in sugarbeets, carrots and cabbage