NO131151B - - Google Patents

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Info

Publication number: NO131151B
Authority: NO; Norway
Prior art keywords: methyl; phenyl; thiocarbamate; compound; solution
Prior art date: 1970-11-24

Application number

NO4303/71A

Other languages

English (en)

Norwegian (no)

Other versions

NO131151C (fi

Inventor

F Arndt

G Boroschewski

Original Assignee

Schering 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.)

1970-11-24

Filing date

1971-11-23

Publication date

1975-01-06

1971-11-23 Application filed by Schering Ag filed Critical Schering Ag

1975-01-06 Publication of NO131151B publication Critical patent/NO131151B/no

1975-04-16 Publication of NO131151C publication Critical patent/NO131151C/no

Links

150000001875 compounds Chemical class 0.000 claims description 12
230000000694 effects Effects 0.000 claims description 7
239000004480 active ingredient Substances 0.000 claims description 6
239000004009 herbicide Substances 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 2
125000005037 alkyl phenyl group Chemical group 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
230000002363 herbicidal effect Effects 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
239000013543 active substance Substances 0.000 description 15
241000196324 Embryophyta Species 0.000 description 14
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
239000000243 solution Substances 0.000 description 11
244000025254 Cannabis sativa Species 0.000 description 8
-1 carbamoyloxyphenylthiocarbamates Chemical class 0.000 description 8
238000002360 preparation method Methods 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000003795 chemical substances by application Substances 0.000 description 6
150000007530 organic bases Chemical class 0.000 description 5
CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
244000062793 Sorghum vulgare Species 0.000 description 3
239000000654 additive Substances 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
150000007529 inorganic bases Chemical class 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000007787 solid Substances 0.000 description 3
CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical class NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
240000007594 Oryza sativa Species 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
125000000066 S-methyl group Chemical group [H]C([H])([H])S* 0.000 description 2
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000002253 acid Substances 0.000 description 2
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical class OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 2
238000001816 cooling Methods 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
229910052943 magnesium sulfate Inorganic materials 0.000 description 2
235000019341 magnesium sulphate Nutrition 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
238000001953 recrystallisation Methods 0.000 description 2
239000002689 soil Substances 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical class OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
YHWQJTNMKZWBBN-UHFFFAOYSA-N 4-ethyl-n-methylaniline Chemical compound CCC1=CC=C(NC)C=C1 YHWQJTNMKZWBBN-UHFFFAOYSA-N 0.000 description 1
125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
240000004385 Centaurea cyanus Species 0.000 description 1
235000005940 Centaurea cyanus Nutrition 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
244000152970 Digitaria sanguinalis Species 0.000 description 1
235000010823 Digitaria sanguinalis Nutrition 0.000 description 1
ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
244000214240 Galinsoga parviflora Species 0.000 description 1
235000018914 Galinsoga parviflora Nutrition 0.000 description 1
241000520028 Lamium Species 0.000 description 1
244000042664 Matricaria chamomilla Species 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
239000007868 Raney catalyst Substances 0.000 description 1
NPXOKRUENSOPAO-UHFFFAOYSA-N Raney nickel Chemical compound [Al].[Ni] NPXOKRUENSOPAO-UHFFFAOYSA-N 0.000 description 1
229910000564 Raney nickel Inorganic materials 0.000 description 1
240000003705 Senecio vulgaris Species 0.000 description 1
240000005498 Setaria italica Species 0.000 description 1
235000007226 Setaria italica Nutrition 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
NXGJISZVWPEFPV-UHFFFAOYSA-N [3-(methylsulfanylcarbonylamino)phenyl] carbonochloridate Chemical compound CSC(=O)NC1=CC=CC(OC(Cl)=O)=C1 NXGJISZVWPEFPV-UHFFFAOYSA-N 0.000 description 1
DXNQLZJOTVNBOZ-UHFFFAOYSA-N [O]C(=O)Nc1ccccc1 Chemical group [O]C(=O)Nc1ccccc1 DXNQLZJOTVNBOZ-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000005215 alkyl ethers Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000008187 granular material Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
150000008040 ionic compounds Chemical class 0.000 description 1
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
239000004571 lime Substances 0.000 description 1
210000001699 lower leg Anatomy 0.000 description 1
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
239000000203 mixture Substances 0.000 description 1
CPGWSLFYXMRNDV-UHFFFAOYSA-N n-methyl-n-phenylcarbamoyl chloride Chemical compound ClC(=O)N(C)C1=CC=CC=C1 CPGWSLFYXMRNDV-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
231100001184 nonphytotoxic Toxicity 0.000 description 1
125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
BMBJSXKEXRFGAV-UHFFFAOYSA-N phenylcarbamothioic s-acid Chemical class SC(=O)NC1=CC=CC=C1 BMBJSXKEXRFGAV-UHFFFAOYSA-N 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
239000000843 powder Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
FZMQIVKTRXXFDS-UHFFFAOYSA-N s-methyl n-(3-hydroxyphenyl)carbamothioate Chemical compound CSC(=O)NC1=CC=CC(O)=C1 FZMQIVKTRXXFDS-UHFFFAOYSA-N 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
235000017557 sodium bicarbonate Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO4303/71A 1970-11-24 1971-11-23 NO131151C (fi)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19702059309 DE2059309A1 (de)	1970-11-24	1970-11-24	Selektives herbizides Mittel

Publications (2)

Publication Number	Publication Date
NO131151B true NO131151B (fi)	1975-01-06
NO131151C NO131151C (fi)	1975-04-16

Family

ID=5789776

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO4303/71A NO131151C (fi)	1970-11-24	1971-11-23

Country Status (29)

Country	Link
JP (1)	JPS5015847B1 (fi)
AT (1)	AT311717B (fi)
AU (1)	AU461419B2 (fi)
BE (1)	BE775754A (fi)
BG (1)	BG20071A3 (fi)
BR (1)	BR7105564D0 (fi)
CA (1)	CA946408A (fi)
CH (1)	CH561009A5 (fi)
CS (1)	CS167323B2 (fi)
DE (1)	DE2059309A1 (fi)
DK (1)	DK128552B (fi)
EG (1)	EG10238A (fi)
ES (1)	ES393926A1 (fi)
FI (1)	FI54219C (fi)
FR (1)	FR2115339B1 (fi)
GB (1)	GB1369491A (fi)
HU (1)	HU163629B (fi)
IE (1)	IE35674B1 (fi)
IL (2)	IL38183A0 (fi)
IT (1)	IT941776B (fi)
LU (1)	LU64313A1 (fi)
NL (1)	NL7116114A (fi)
NO (1)	NO131151C (fi)
OA (1)	OA03840A (fi)
PH (1)	PH11826A (fi)
PL (1)	PL81438B1 (fi)
RO (2)	RO62289A2 (fi)
YU (1)	YU35351B (fi)
ZA (1)	ZA715706B (fi)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2310649C3 (de) *	1973-03-01	1982-05-06	Schering Ag, 1000 Berlin Und 4619 Bergkamen	Diurethane sowie diese enthaltende selektive herbizide Mittel

1970
- 1970-11-24 DE DE19702059309 patent/DE2059309A1/de not_active Withdrawn
1971
- 1971-06-18 DK DK301571AA patent/DK128552B/da not_active IP Right Cessation
- 1971-06-25 YU YU1660/71A patent/YU35351B/xx unknown
- 1971-07-20 FI FI2057/71A patent/FI54219C/fi active
- 1971-07-28 CS CS5527A patent/CS167323B2/cs unknown
- 1971-08-05 ES ES393926A patent/ES393926A1/es not_active Expired
- 1971-08-11 PH PH12743A patent/PH11826A/en unknown
- 1971-08-16 BG BG18353A patent/BG20071A3/xx unknown
- 1971-08-25 BR BR5564/71A patent/BR7105564D0/pt unknown
- 1971-08-26 ZA ZA715706A patent/ZA715706B/xx unknown
- 1971-09-27 GB GB4494571A patent/GB1369491A/en not_active Expired
- 1971-09-28 IE IE1210/71A patent/IE35674B1/xx unknown
- 1971-09-30 CA CA124,101A patent/CA946408A/en not_active Expired
- 1971-10-01 RO RO68336A patent/RO62289A2/ro unknown
- 1971-10-01 RO RO76243A patent/RO62664A2/ro unknown
- 1971-11-15 EG EG498/71A patent/EG10238A/xx active
- 1971-11-15 AU AU35714/71A patent/AU461419B2/en not_active Expired
- 1971-11-19 IL IL38183A patent/IL38183A0/xx unknown
- 1971-11-22 CH CH1697271A patent/CH561009A5/xx not_active IP Right Cessation
- 1971-11-22 LU LU64313D patent/LU64313A1/xx unknown
- 1971-11-22 PL PL1971151698A patent/PL81438B1/pl unknown
- 1971-11-23 FR FR7141818A patent/FR2115339B1/fr not_active Expired
- 1971-11-23 NL NL7116114A patent/NL7116114A/xx not_active Application Discontinuation
- 1971-11-23 OA OA54416A patent/OA03840A/xx unknown
- 1971-11-23 AT AT1007871A patent/AT311717B/de not_active IP Right Cessation
- 1971-11-23 NO NO4303/71A patent/NO131151C/no unknown
- 1971-11-23 HU HUSCHE364*1A patent/HU163629B/hu unknown
- 1971-11-24 JP JP46094400A patent/JPS5015847B1/ja active Pending
- 1971-11-24 IT IT31542/71A patent/IT941776B/it active
- 1971-11-24 BE BE775754A patent/BE775754A/xx not_active IP Right Cessation
1974
- 1974-11-19 IL IL38183A patent/IL38183A/en unknown

Also Published As

Publication number	Publication date
NO131151C (fi)	1975-04-16
AU461419B2 (en)	1975-05-08
IE35674B1 (en)	1976-04-14
JPS5015847B1 (fi)	1975-06-09
EG10238A (en)	1976-05-31
BE775754A (fr)	1972-05-24
YU35351B (en)	1980-12-31
FR2115339B1 (fi)	1976-04-02
CA946408A (en)	1974-04-30
DE2059309A1 (de)	1972-09-07
LU64313A1 (fi)	1972-06-13
AT311717B (de)	1973-11-26
FI54219B (fi)	1978-07-31
PH11826A (en)	1978-07-19
NL7116114A (fi)	1972-05-26
ES393926A1 (es)	1973-11-01
BR7105564D0 (pt)	1973-02-15
IT941776B (it)	1973-03-10
ZA715706B (en)	1972-04-26
BG20071A3 (fi)	1975-10-30
DK128552B (da)	1974-05-27
FI54219C (fi)	1978-11-10
AU3571471A (en)	1973-05-24
YU166071A (en)	1980-06-30
CH561009A5 (fi)	1975-04-30
HU163629B (fi)	1973-09-27
GB1369491A (en)	1974-10-09
FR2115339A1 (fi)	1972-07-07
RO62664A2 (ro)	1978-01-30
PL81438B1 (fi)	1975-08-30
SU361538A3 (fi)	1972-12-07
OA03840A (fr)	1971-12-24
CS167323B2 (fi)	1976-04-29
IL38183A (en)	1974-12-31
IL38183A0 (en)	1972-01-27
IE35674L (en)	1972-05-24
RO62289A2 (ro)	1977-09-05

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DE69932628T2 (de)	2006-12-14	Herbizide
US5324854A (en)	1994-06-28	Intermediate isocyana to benzenesulfonamide compounds
SI9300627A (en)	1994-06-30	Selective herbicid comprising pyridinsulphonylureas and sulphamoylphenylureas
US4149872A (en)	1979-04-17	N-pyridinyl urea and cyclopropanecarboxamide herbicides
JPS62292773A (ja)	1987-12-19	トリ置換された１，３，５−トリアジン−２，４，６−トリオン類
DE69126836T2 (de)	1998-01-02	Herbizide
JPS59212490A (ja)	1984-12-01	縮合したｎ−フエニルスルホニル−ｎ′−ピリミジニル尿素及びｎ−フエニルスルホニル−ｎ′−トリアジニル尿素、その製法、中間体、組成物及び使用法
JPH04235984A (ja)	1992-08-25	新規なスルホニル尿素
US3535101A (en)	1970-10-20	Herbicide and algicide means
EP0103537A2 (de)	1984-03-21	N-Arylsulfonyl-N'-triazolylharnstoffe
NO176714B (no)	1995-02-06	Herbicide [[(1,3,5-triazin-2-yl)aminokarbonylÅ-aminosulfonylÅbenzosyreestere og herbicid middel, og anvendelse av disse
JPS6036467A (ja)	1985-02-25	置換フエニルスルホニルグアニジン誘導体、その中間体、それらの製法及び雑草防除剤
NO131151B (fi)	1975-01-06
NO157025B (no)	1987-09-28	Fremgangsmte for fremstilling av zr eller hf ved elektrolyse samt celle for gjennomfring av fremgangsmten.
EP0057367B1 (de)	1983-12-28	2-Pyridyloxyacetanilid-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung
EP0062254A1 (de)	1982-10-13	Substituierte Acetanilide, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide
US3512955A (en)	1970-05-19	Method of protecting plant growth
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