NO823837L - Thiazolo- og (1,3)thiazino(2,3-c)(1,2,4)triazinoner med selektiv herbicid virkning - Google Patents

Thiazolo- og (1,3)thiazino(2,3-c)(1,2,4)triazinoner med selektiv herbicid virkning

Info

Publication number: NO823837L
Authority: NO; Norway
Prior art keywords: general formula; compounds; thiazolo; residue; triazin
Prior art date: 1981-11-17

Application number

NO823837A

Other languages

English (en)

Norwegian (no)

Inventor

Walter Klose

Friedrich Arndt

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.)

1981-11-17

Filing date

1982-11-16

Publication date

1983-05-18

1982-11-16 Application filed by Schering Ag filed Critical Schering Ag

1983-05-18 Publication of NO823837L publication Critical patent/NO823837L/no

Links

239000004009 herbicide Substances 0.000 title claims description 9
230000002363 herbicidal effect Effects 0.000 title description 8
230000000694 effects Effects 0.000 title description 5
150000001875 compounds Chemical class 0.000 claims description 57
-1 alkyl radical Chemical class 0.000 claims description 46
150000002148 esters Chemical group 0.000 claims description 19
239000001257 hydrogen Substances 0.000 claims description 15
229910052739 hydrogen Inorganic materials 0.000 claims description 15
150000002431 hydrogen Chemical class 0.000 claims description 13
238000000034 method Methods 0.000 claims description 13
239000002253 acid Substances 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
150000004945 aromatic hydrocarbons Chemical group 0.000 claims description 8
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 8
238000004440 column chromatography Methods 0.000 claims description 7
230000015572 biosynthetic process Effects 0.000 claims description 4
238000004519 manufacturing process Methods 0.000 claims description 4
XAPZGOGOGZTORK-UHFFFAOYSA-N 3-phenyl-6,7-dihydro-[1,3]thiazolo[2,3-c][1,2,4]triazin-4-one Chemical compound N=1N=C2SCCN2C(=O)C=1C1=CC=CC=C1 XAPZGOGOGZTORK-UHFFFAOYSA-N 0.000 claims description 3
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 3
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
150000001991 dicarboxylic acids Chemical class 0.000 claims description 3
BRWIZMBXBAOCCF-UHFFFAOYSA-N hydrazinecarbothioamide Chemical compound NNC(N)=S BRWIZMBXBAOCCF-UHFFFAOYSA-N 0.000 claims description 3
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 3
125000001544 thienyl group Chemical group 0.000 claims description 3
JBZQTXHRAJTBHF-UHFFFAOYSA-N 3-methyl-6,7-dihydro-[1,3]thiazolo[2,3-c][1,2,4]triazin-4-one Chemical compound O=C1C(C)=NN=C2SCCN21 JBZQTXHRAJTBHF-UHFFFAOYSA-N 0.000 claims description 2
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
125000003118 aryl group Chemical group 0.000 claims description 2
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125000000068 chlorophenyl group Chemical group 0.000 claims description 2
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229910052760 oxygen Inorganic materials 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
125000003944 tolyl group Chemical group 0.000 claims description 2
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims 1
PSVPVRSPYGEGDQ-UHFFFAOYSA-N 3-cyclohexyl-6,7-dihydro-[1,3]thiazolo[2,3-c][1,2,4]triazin-4-one Chemical compound C1(CCCCC1)C=1C(N2C(=NN1)SCC2)=O PSVPVRSPYGEGDQ-UHFFFAOYSA-N 0.000 claims 1
GZPLWCGOPQWQGE-UHFFFAOYSA-N 3-cyclopentyl-6,7-dihydro-[1,3]thiazolo[2,3-c][1,2,4]triazin-4-one Chemical compound C1(CCCC1)C=1C(N2C(=NN1)SCC2)=O GZPLWCGOPQWQGE-UHFFFAOYSA-N 0.000 claims 1
GHBIFHZRNCZXLR-UHFFFAOYSA-N 6-methyl-3-phenyl-6,7-dihydro-[1,3]thiazolo[2,3-c][1,2,4]triazin-4-one Chemical compound C1(=CC=CC=C1)C=1C(N2C(=NN1)SCC2C)=O GHBIFHZRNCZXLR-UHFFFAOYSA-N 0.000 claims 1
125000003545 alkoxy group Chemical group 0.000 claims 1
229910052736 halogen Inorganic materials 0.000 claims 1
150000002367 halogens Chemical class 0.000 claims 1
QKAJPXJSGSKBRV-UHFFFAOYSA-N methyl 2-(4-oxo-6,7-dihydro-[1,3]thiazolo[2,3-c][1,2,4]triazin-3-yl)acetate Chemical compound C(=O)(OC)CC=1C(N2C(=NN1)SCC2)=O QKAJPXJSGSKBRV-UHFFFAOYSA-N 0.000 claims 1
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239000004480 active ingredient Substances 0.000 description 6
239000002585 base Substances 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
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229910002027 silica gel Inorganic materials 0.000 description 6
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150000007513 acids Chemical class 0.000 description 5
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HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
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239000005457 ice water Substances 0.000 description 4
235000017557 sodium bicarbonate Nutrition 0.000 description 4
229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
239000002689 soil Substances 0.000 description 4
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VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 4
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159000000007 calcium salts Chemical class 0.000 description 3
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YLHXLHGIAMFFBU-UHFFFAOYSA-N methyl phenylglyoxalate Chemical compound COC(=O)C(=O)C1=CC=CC=C1 YLHXLHGIAMFFBU-UHFFFAOYSA-N 0.000 description 3
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239000000047 product Substances 0.000 description 3
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239000000725 suspension Substances 0.000 description 3
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APQIUTYORBAGEZ-UHFFFAOYSA-N 1,1-dibromoethane Chemical compound CC(Br)Br APQIUTYORBAGEZ-UHFFFAOYSA-N 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
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LYKSBPASYCQKJE-UHFFFAOYSA-N 6-methyl-3-phenyl-[1,3]thiazolo[2,3-c][1,2,4]triazin-4-one Chemical compound O=C1N2C(C)=CSC2=NN=C1C1=CC=CC=C1 LYKSBPASYCQKJE-UHFFFAOYSA-N 0.000 description 2
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235000010469 Glycine max Nutrition 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
235000019738 Limestone Nutrition 0.000 description 1
235000011999 Panicum crusgalli Nutrition 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
241000220261 Sinapis Species 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
235000002634 Solanum Nutrition 0.000 description 1
241000207763 Solanum Species 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
241000405217 Viola <butterfly> Species 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
GUDKUSFHFHUXSZ-UHFFFAOYSA-N [1,3]thiazolo[2,3-c][1,2,4]triazin-4-one Chemical compound N=1N=CC(N2C1SC=C2)=O GUDKUSFHFHUXSZ-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
150000003931 anilides Chemical class 0.000 description 1
150000001448 anilines Chemical class 0.000 description 1
229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
150000008107 benzenesulfonic acids Chemical class 0.000 description 1
125000003785 benzimidazolyl group Chemical class N1=C(NC2=C1C=CC=C2)* 0.000 description 1
150000005130 benzoxazines Chemical class 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
150000004657 carbamic acid derivatives Chemical class 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
150000001733 carboxylic acid esters Chemical group 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000001816 cooling Methods 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000002178 crystalline material Substances 0.000 description 1
125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
150000002019 disulfides Chemical class 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
150000004659 dithiocarbamates Chemical class 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000008187 granular material Substances 0.000 description 1
230000012010 growth Effects 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000001469 hydantoins Chemical class 0.000 description 1
229940042795 hydrazides for tuberculosis treatment Drugs 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
150000002460 imidazoles Chemical group 0.000 description 1
238000010348 incorporation Methods 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000006028 limestone Substances 0.000 description 1
KXKVLQRXCPHEJC-UHFFFAOYSA-N methyl acetate Chemical group COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
CWKLZLBVOJRSOM-UHFFFAOYSA-N methyl pyruvate Chemical compound COC(=O)C(C)=O CWKLZLBVOJRSOM-UHFFFAOYSA-N 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
238000002156 mixing Methods 0.000 description 1
125000006606 n-butoxy group Chemical group 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
150000002791 naphthoquinones Chemical class 0.000 description 1
125000006501 nitrophenyl group Chemical group 0.000 description 1
231100001184 nonphytotoxic Toxicity 0.000 description 1
230000009965 odorless effect Effects 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
QNMLMAVEXUCXRG-UHFFFAOYSA-N oxadiazinane-4,5-dione Chemical class O=C1CONNC1=O QNMLMAVEXUCXRG-UHFFFAOYSA-N 0.000 description 1
SDRLFDJOSQLRPB-UHFFFAOYSA-N oxadiazine-4,5-dione Chemical class O=C1CON=NC1=O SDRLFDJOSQLRPB-UHFFFAOYSA-N 0.000 description 1
150000004866 oxadiazoles Chemical class 0.000 description 1
JPILDORBIJCDHE-UHFFFAOYSA-N oxadiazolidin-4-one Chemical class O=C1CONN1 JPILDORBIJCDHE-UHFFFAOYSA-N 0.000 description 1
YDCVQGAUCOROHB-UHFFFAOYSA-N oxadiazolidine-4,5-dione Chemical class O=C1NNOC1=O YDCVQGAUCOROHB-UHFFFAOYSA-N 0.000 description 1
LIGACIXOYTUXAW-UHFFFAOYSA-N phenacyl bromide Chemical compound BrCC(=O)C1=CC=CC=C1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical compound OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 description 1
REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical class P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 description 1
AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
150000003053 piperidines Chemical class 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
238000000746 purification Methods 0.000 description 1
150000003217 pyrazoles Chemical class 0.000 description 1
BFZYLUGEHGYJKJ-UHFFFAOYSA-N pyrazolidine-3-thione Chemical class S=C1CCNN1 BFZYLUGEHGYJKJ-UHFFFAOYSA-N 0.000 description 1
150000004892 pyridazines Chemical class 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
150000005299 pyridinones Chemical class 0.000 description 1
150000003230 pyrimidines Chemical class 0.000 description 1
150000008318 pyrimidones Chemical class 0.000 description 1
NYCVCXMSZNOGDH-UHFFFAOYSA-N pyrrolidine-1-carboxylic acid Chemical class OC(=O)N1CCCC1 NYCVCXMSZNOGDH-UHFFFAOYSA-N 0.000 description 1
150000003235 pyrrolidines Chemical class 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
125000002294 quinazolinyl group Chemical class N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
150000003248 quinolines Chemical class 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
230000021749 root development Effects 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
238000009331 sowing Methods 0.000 description 1
241000894007 species Species 0.000 description 1
239000007921 spray Substances 0.000 description 1
125000003011 styrenyl group Chemical class [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
150000003462 sulfoxides Chemical class 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
150000004867 thiadiazoles Chemical class 0.000 description 1
OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical class O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 0.000 description 1
SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical compound CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
150000003566 thiocarboxylic acids Chemical class 0.000 description 1
150000003582 thiophosphoric acids Chemical class 0.000 description 1
150000003585 thioureas Chemical class 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
150000007968 uric acids Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
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)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

NO823837A 1981-11-17 1982-11-16 Thiazolo- og (1,3)thiazino(2,3-c)(1,2,4)triazinoner med selektiv herbicid virkning NO823837L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19813146299 DE3146299A1 (de)	1981-11-17	1981-11-17	Thiazolo- und (1,3)thiazino(2,3-c)(1,2,4)triazinone mit selektiver herbizider wirkung sowie verfahren zur herstellung dieser verbindungen

Publications (1)

Publication Number	Publication Date
NO823837L true NO823837L (no)	1983-05-18

Family

ID=6146966

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO823837A NO823837L (no)	1981-11-17	1982-11-16	Thiazolo- og (1,3)thiazino(2,3-c)(1,2,4)triazinoner med selektiv herbicid virkning

Country Status (25)

Country	Link
JP (1)	JPS6030645B2 (de)
AU (1)	AU9024482A (de)
BE (1)	BE895027A (de)
BR (1)	BR8206610A (de)
CS (1)	CS818282A2 (de)
DD (1)	DD204024A5 (de)
DE (1)	DE3146299A1 (de)
DK (1)	DK487182A (de)
ES (1)	ES8307828A1 (de)
FI (1)	FI823382A0 (de)
FR (1)	FR2516516A1 (de)
GB (1)	GB2109792A (de)
IL (1)	IL67189A0 (de)
IN (1)	IN158962B (de)
IT (1)	IT1191079B (de)
LU (1)	LU84476A1 (de)
NL (1)	NL8204034A (de)
NO (1)	NO823837L (de)
OA (1)	OA07251A (de)
PL (1)	PL131798B1 (de)
PT (1)	PT75855B (de)
SE (1)	SE8206524L (de)
TR (1)	TR21697A (de)
YU (1)	YU217682A (de)
ZA (1)	ZA828471B (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH04292009A (ja) *	1991-03-20	1992-10-16	Mitsubishi Electric Corp	高周波線形増幅器
TW221689B (de) *	1991-08-27	1994-03-11	Otsuka Pharma Co Ltd
RU2766696C1 (ru) *	2021-06-10	2022-03-15	Федеральное государственное бюджетное образовательное учреждение высшего образования "Уфимский государственный нефтяной технический университет"	Производные 1,2,4-триазинонов, проявляющие гербицидную активность

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CH495110A (de)	1966-04-16	1970-08-31	Bayer Ag	Herbizides Mittel
US3887679A (en)	1972-05-31	1975-06-03	Falconbridge Nickel Mines Ltd	Separation of copper from cobalt

1981
- 1981-11-17 DE DE19813146299 patent/DE3146299A1/de not_active Withdrawn
1982
- 1982-09-28 YU YU02176/82A patent/YU217682A/xx unknown
- 1982-10-05 FI FI823382A patent/FI823382A0/fi not_active Application Discontinuation
- 1982-10-19 NL NL8204034A patent/NL8204034A/nl not_active Application Discontinuation
- 1982-11-02 IN IN797/DEL/82A patent/IN158962B/en unknown
- 1982-11-03 DK DK487182A patent/DK487182A/da not_active Application Discontinuation
- 1982-11-05 TR TR21697A patent/TR21697A/xx unknown
- 1982-11-05 IL IL67189A patent/IL67189A0/xx unknown
- 1982-11-08 AU AU90244/82A patent/AU9024482A/en not_active Abandoned
- 1982-11-11 JP JP57196863A patent/JPS6030645B2/ja not_active Expired
- 1982-11-12 DD DD82244831A patent/DD204024A5/de unknown
- 1982-11-12 BR BR8206610A patent/BR8206610A/pt unknown
- 1982-11-15 PT PT75855A patent/PT75855B/de unknown
- 1982-11-15 IT IT24249/82A patent/IT1191079B/it active
- 1982-11-15 PL PL1982239047A patent/PL131798B1/pl unknown
- 1982-11-16 GB GB08232647A patent/GB2109792A/en not_active Withdrawn
- 1982-11-16 SE SE8206524A patent/SE8206524L/xx not_active Application Discontinuation
- 1982-11-16 NO NO823837A patent/NO823837L/no unknown
- 1982-11-16 ES ES517409A patent/ES8307828A1/es not_active Expired
- 1982-11-16 BE BE0/209487A patent/BE895027A/fr not_active IP Right Cessation
- 1982-11-16 OA OA57844A patent/OA07251A/xx unknown
- 1982-11-17 LU LU84476A patent/LU84476A1/de unknown
- 1982-11-17 ZA ZA828471A patent/ZA828471B/xx unknown
- 1982-11-17 CS CS828182A patent/CS818282A2/cs unknown
- 1982-11-17 FR FR8219206A patent/FR2516516A1/fr active Pending

Also Published As

Publication number	Publication date
JPS5892601A (ja)	1983-06-02
PL239047A1 (en)	1983-08-01
BR8206610A (pt)	1983-10-04
ZA828471B (en)	1983-09-28
YU217682A (en)	1984-12-31
DK487182A (da)	1983-05-18
FR2516516A1 (fr)	1983-05-20
IL67189A0 (en)	1983-03-31
AU9024482A (en)	1983-05-26
IN158962B (de)	1987-02-28
IT1191079B (it)	1988-02-24
PT75855A (de)	1982-12-01
FI823382A0 (fi)	1982-10-05
IT8224249A0 (it)	1982-11-15
OA07251A (fr)	1984-04-30
TR21697A (tr)	1985-03-05
JPS6030645B2 (ja)	1985-07-17
NL8204034A (nl)	1983-06-16
ES517409A0 (es)	1983-08-01
PL131798B1 (en)	1985-01-31
ES8307828A1 (es)	1983-08-01
SE8206524D0 (sv)	1982-11-16
DD204024A5 (de)	1983-11-16
CS818282A2 (en)	1985-06-13
LU84476A1 (de)	1983-06-13
GB2109792A (en)	1983-06-08
BE895027A (fr)	1983-05-16
SE8206524L (sv)	1983-05-18
DE3146299A1 (de)	1983-06-01
PT75855B (de)	1985-10-04

Publication	Publication Date	Title
AP131A (en)	1991-04-20	Fungicides.
DE69104071T2 (de)	1995-05-11	Uracilderivate und Pestizide, die diese als wirksame Stoffe enthalten.
US5447945A (en)	1995-09-05	Nematicidal compositions
US3823135A (en)	1974-07-09	Pyrimidone herbicides
SK287483B6 (sk)	2010-11-08	Substituované pyridíny, spôsob ich prípravy, herbicídna a rast rastlín inhibujúca kompozícia a ich použitie
US4561880A (en)	1985-12-31	1H[1,2,4]-Triazolo[1,2-a]pyridazine-1,3-diones useful as herbicides
AU595229B2 (en)	1990-03-29	Substituted semicarbazones, thiosemicarbazones and isothiosemicarbazones
NZ199882A (en)	1985-05-31	N-heterocyclyl-methyl-amide derivatives and fungicidal and herbicidal compositions
DE69110093T2 (de)	1995-10-19	Pyrimidinderivate.
AU607798B2 (en)	1991-03-14	Novel pyrrolidine-2,5-diones and 4,5,6,7-tetrahydroisoindole-1,3-diones
US3828043A (en)	1974-08-06	5-acyl barbituric acid derivatives
US3967950A (en)	1976-07-06	Combating weeds in rice with benzothiazole derivatives
NO823837L (no)	1983-05-18	Thiazolo- og (1,3)thiazino(2,3-c)(1,2,4)triazinoner med selektiv herbicid virkning
US4072495A (en)	1978-02-07	5-Benzofuranyl esters as herbicides and plant growth regulants
US3993771A (en)	1976-11-23	α-Benzylidene lactone derivatives
JPH04145081A (ja)	1992-05-19	ピラゾールカルボン酸誘導体及び除草剤
CZ28796A3 (en)	1996-08-14	/1,3,4/oxadiazoles and thiadiazoles as well as herbicidal agents based thereon
JPH02286665A (ja)	1990-11-26	殺菌剤
US4345932A (en)	1982-08-24	Herbicides
JPH0248572A (ja)	1990-02-19	新規なチアゾール化合物及びその製造方法並びに該化合物を有効成分とする殺菌剤組成物
US4120871A (en)	1978-10-17	5-Organosulfonyl, 5-organosulfinyl or 5-haloalkanoyl-benzofuran-2-ones
US4249933A (en)	1981-02-10	Herbicidal agents containing a thiolcarbamate
US3758481A (en)	1973-09-11	Ridine m-(2,4-dichloro - 5-(haloalkoxy)-phenylcarbomoyl)-pyrrolidine or pipe
NO811258L (no)	1981-04-13	Fungicide, heterocyklisk substituerte tioglykolsyreanilider, fremgangsmaate til deres fremstilling og skadedyrs-bekjempelsesmidler inneholdende disse
EP0562575A2 (de)	1993-09-29	N-substituierte-3-(substituierte Hydrazino)-Benzolsulfonamidderivate, Verfahren zur Herstellung und herbizide Zusammensetzungen