NL8203767A - Carbonzuuramidothiolcarbamaatderivaten bevattend onkruidbestrijdingsmiddel en werkwijze voor de bereiding van de actieve stoffen. - Google Patents

Carbonzuuramidothiolcarbamaatderivaten bevattend onkruidbestrijdingsmiddel en werkwijze voor de bereiding van de actieve stoffen. Download PDF

Info

Publication number: NL8203767A
Authority: NL; Netherlands
Prior art keywords: ethyl; phenyl; carbon atoms; propyl; butyl
Prior art date: 1981-09-29

Application number

NL8203767A

Other languages

English (en)

Dutch (nl)

Original Assignee

Eszakmagyar Vegyimuevek

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.)

1981-09-29

Filing date

1982-09-29

Publication date

1983-04-18

1982-09-29 Application filed by Eszakmagyar Vegyimuevek filed Critical Eszakmagyar Vegyimuevek

1983-04-18 Publication of NL8203767A publication Critical patent/NL8203767A/nl

Links

241000196324 Embryophyta Species 0.000 title claims description 47
239000013543 active substance Substances 0.000 title claims description 24
238000000034 method Methods 0.000 title claims description 7
150000004657 carbamic acid derivatives Chemical class 0.000 title claims description 4
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 title 1
239000000126 substance Substances 0.000 claims description 73
125000004432 carbon atom Chemical group C* 0.000 claims description 32
239000000203 mixture Substances 0.000 claims description 29
238000002360 preparation method Methods 0.000 claims description 28
-1 alkyl radical Chemical class 0.000 claims description 26
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 17
150000001875 compounds Chemical class 0.000 claims description 12
150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 10
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 9
239000007787 solid Substances 0.000 claims description 8
125000003342 alkenyl group Chemical group 0.000 claims description 7
239000007788 liquid Substances 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
239000004094 surface-active agent Substances 0.000 claims description 7
239000000080 wetting agent Substances 0.000 claims description 7
239000002270 dispersing agent Substances 0.000 claims description 6
229910052500 inorganic mineral Inorganic materials 0.000 claims description 5
239000011707 mineral Substances 0.000 claims description 5
239000003921 oil Substances 0.000 claims description 5
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims description 5
235000012239 silicon dioxide Nutrition 0.000 claims description 5
SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 4
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 4
125000000753 cycloalkyl group Chemical group 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
239000003960 organic solvent Substances 0.000 claims description 4
239000011541 reaction mixture Substances 0.000 claims description 4
239000002904 solvent Substances 0.000 claims description 4
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
125000005843 halogen group Chemical group 0.000 claims description 3
125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 claims description 3
AKZWRTCWNXHHFR-PDIZUQLASA-N [(3S)-oxolan-3-yl] N-[(2S,3S)-4-[(5S)-5-benzyl-3-[(2R)-2-carbamoyloxy-2,3-dihydro-1H-inden-1-yl]-4-oxo-3H-pyrrol-5-yl]-3-hydroxy-1-phenylbutan-2-yl]carbamate Chemical compound NC(=O)O[C@@H]1Cc2ccccc2C1C1C=N[C@](C[C@H](O)[C@H](Cc2ccccc2)NC(=O)O[C@H]2CCOC2)(Cc2ccccc2)C1=O AKZWRTCWNXHHFR-PDIZUQLASA-N 0.000 claims description 2
239000002736 nonionic surfactant Substances 0.000 claims 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 2
125000000129 anionic group Chemical group 0.000 claims 2
239000003945 anionic surfactant Substances 0.000 claims 2
150000004945 aromatic hydrocarbons Chemical class 0.000 claims 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 claims 2
150000008282 halocarbons Chemical class 0.000 claims 2
229940088623 biologically active substance Drugs 0.000 claims 1
125000002091 cationic group Chemical group 0.000 claims 1
229910021653 sulphate ion Inorganic materials 0.000 claims 1
238000009736 wetting Methods 0.000 claims 1
239000004563 wettable powder Substances 0.000 description 23
238000012360 testing method Methods 0.000 description 19
238000003756 stirring Methods 0.000 description 12
239000000729 antidote Substances 0.000 description 10
230000006378 damage Effects 0.000 description 10
238000011282 treatment Methods 0.000 description 10
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
240000008042 Zea mays Species 0.000 description 9
235000013339 cereals Nutrition 0.000 description 9
239000012141 concentrate Substances 0.000 description 8
239000000839 emulsion Substances 0.000 description 8
244000020551 Helianthus annuus Species 0.000 description 7
235000003222 Helianthus annuus Nutrition 0.000 description 7
239000004009 herbicide Substances 0.000 description 7
239000002689 soil Substances 0.000 description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
GUVLYNGULCJVDO-UHFFFAOYSA-N EPTC Chemical compound CCCN(CCC)C(=O)SCC GUVLYNGULCJVDO-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
235000002017 Zea mays subsp mays Nutrition 0.000 description 6
239000011324 bead Substances 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 5
YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000011734 sodium Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
ZRYCRPNCXLQHPN-UHFFFAOYSA-N 3-hydroxy-2-methylbenzaldehyde Chemical compound CC1=C(O)C=CC=C1C=O ZRYCRPNCXLQHPN-UHFFFAOYSA-N 0.000 description 4
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 4
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 description 4
240000007594 Oryza sativa Species 0.000 description 4
235000007164 Oryza sativa Nutrition 0.000 description 4
241000218206 Ranunculus Species 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000012153 distilled water Substances 0.000 description 4
238000011049 filling Methods 0.000 description 4
238000007667 floating Methods 0.000 description 4
238000004817 gas chromatography Methods 0.000 description 4
239000011521 glass Substances 0.000 description 4
230000002363 herbicidal effect Effects 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000004576 sand Substances 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
240000002791 Brassica napus Species 0.000 description 3
240000001980 Cucurbita pepo Species 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
240000006240 Linum usitatissimum Species 0.000 description 3
235000004431 Linum usitatissimum Nutrition 0.000 description 3
235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
235000005775 Setaria Nutrition 0.000 description 3
241000232088 Setaria <nematode> Species 0.000 description 3
240000003768 Solanum lycopersicum Species 0.000 description 3
244000062793 Sorghum vulgare Species 0.000 description 3
241000209140 Triticum Species 0.000 description 3
235000021307 Triticum Nutrition 0.000 description 3
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000008346 aqueous phase Substances 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
SMLHHBQGIJMAIM-UHFFFAOYSA-N calcium;2-dodecylbenzenesulfonic acid Chemical compound [Ca].CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O SMLHHBQGIJMAIM-UHFFFAOYSA-N 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
239000003995 emulsifying agent Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
235000009973 maize Nutrition 0.000 description 3
239000012074 organic phase Substances 0.000 description 3
230000000885 phytotoxic effect Effects 0.000 description 3
239000004476 plant protection product Substances 0.000 description 3
229920000151 polyglycol Polymers 0.000 description 3
239000010695 polyglycol Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
235000009566 rice Nutrition 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000000725 suspension Substances 0.000 description 3
229910002029 synthetic silica gel Inorganic materials 0.000 description 3
VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 2
235000000832 Ayote Nutrition 0.000 description 2
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
235000004977 Brassica sinapistrum Nutrition 0.000 description 2
244000241257 Cucumis melo Species 0.000 description 2
235000015510 Cucumis melo subsp melo Nutrition 0.000 description 2
235000009854 Cucurbita moschata Nutrition 0.000 description 2
235000009804 Cucurbita pepo subsp pepo Nutrition 0.000 description 2
240000005702 Galium aparine Species 0.000 description 2
235000014820 Galium aparine Nutrition 0.000 description 2
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
RSPISYXLHRIGJD-UHFFFAOYSA-N OOOO Chemical compound OOOO RSPISYXLHRIGJD-UHFFFAOYSA-N 0.000 description 2
RTYZCUMXOXNVSI-UHFFFAOYSA-N OOOOOOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOOOOOO RTYZCUMXOXNVSI-UHFFFAOYSA-N 0.000 description 2
ZMAKCCXIFPCMEE-UHFFFAOYSA-N OOOOOOOOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOOOOOOOO ZMAKCCXIFPCMEE-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
229920003171 Poly (ethylene oxide) Polymers 0.000 description 2
241000219000 Populus Species 0.000 description 2
241000220259 Raphanus Species 0.000 description 2
235000006140 Raphanus sativus var sativus Nutrition 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
235000021536 Sugar beet Nutrition 0.000 description 2
235000007244 Zea mays Nutrition 0.000 description 2
FJJCIZWZNKZHII-UHFFFAOYSA-N [4,6-bis(cyanoamino)-1,3,5-triazin-2-yl]cyanamide Chemical compound N#CNC1=NC(NC#N)=NC(NC#N)=N1 FJJCIZWZNKZHII-UHFFFAOYSA-N 0.000 description 2
239000002671 adjuvant Substances 0.000 description 2
AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 description 2
JYIMWRSJCRRYNK-UHFFFAOYSA-N dialuminum;disodium;oxygen(2-);silicon(4+);hydrate Chemical compound O.[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Na+].[Na+].[Al+3].[Al+3].[Si+4] JYIMWRSJCRRYNK-UHFFFAOYSA-N 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000003864 humus Substances 0.000 description 2
239000003350 kerosene Substances 0.000 description 2
235000012054 meals Nutrition 0.000 description 2
235000019713 millet Nutrition 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 2
235000019271 petrolatum Nutrition 0.000 description 2
239000012071 phase Substances 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
235000015136 pumpkin Nutrition 0.000 description 2
238000011160 research Methods 0.000 description 2
230000002441 reversible effect Effects 0.000 description 2
229910052938 sodium sulfate Inorganic materials 0.000 description 2
235000011152 sodium sulphate Nutrition 0.000 description 2
230000004936 stimulating effect Effects 0.000 description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
238000010998 test method Methods 0.000 description 2
150000003573 thiols Chemical class 0.000 description 2
239000008096 xylene Substances 0.000 description 2
241000219144 Abutilon Species 0.000 description 1
240000002234 Allium sativum Species 0.000 description 1
235000021533 Beta vulgaris Nutrition 0.000 description 1
241000335053 Beta vulgaris Species 0.000 description 1
235000011293 Brassica napus Nutrition 0.000 description 1
235000005940 Centaurea cyanus Nutrition 0.000 description 1
244000241235 Citrullus lanatus Species 0.000 description 1
235000009831 Citrullus lanatus Nutrition 0.000 description 1
235000009852 Cucurbita pepo Nutrition 0.000 description 1
241001101998 Galium Species 0.000 description 1
KUGRPPRAQNPSQD-UHFFFAOYSA-N OOOOO Chemical compound OOOOO KUGRPPRAQNPSQD-UHFFFAOYSA-N 0.000 description 1
OZBZONOEYUBXTD-UHFFFAOYSA-N OOOOOOOOO Chemical compound OOOOOOOOO OZBZONOEYUBXTD-UHFFFAOYSA-N 0.000 description 1
FYKAKDPHDGCKTF-UHFFFAOYSA-N OOOOOOOOOOOOOOOOOOO Chemical compound OOOOOOOOOOOOOOOOOOO FYKAKDPHDGCKTF-UHFFFAOYSA-N 0.000 description 1
239000004264 Petrolatum Substances 0.000 description 1
244000286177 Raphanus raphanistrum Species 0.000 description 1
235000000241 Raphanus raphanistrum Nutrition 0.000 description 1
235000007230 Sorghum bicolor Nutrition 0.000 description 1
240000002439 Sorghum halepense Species 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
241000607479 Yersinia pestis Species 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
XCSGPAVHZFQHGE-UHFFFAOYSA-N alachlor Chemical compound CCC1=CC=CC(CC)=C1N(COC)C(=O)CCl XCSGPAVHZFQHGE-UHFFFAOYSA-N 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
230000002528 anti-freeze Effects 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
238000009395 breeding Methods 0.000 description 1
230000001488 breeding effect Effects 0.000 description 1
230000035601 cold sensitivity Effects 0.000 description 1
229940126214 compound 3 Drugs 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
238000011161 development Methods 0.000 description 1
229960005215 dichloroacetic acid Drugs 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
235000004426 flaxseed Nutrition 0.000 description 1
230000009969 flowable effect Effects 0.000 description 1
238000009472 formulation Methods 0.000 description 1
235000004611 garlic Nutrition 0.000 description 1
229910052602 gypsum Inorganic materials 0.000 description 1
239000010440 gypsum Substances 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
238000005259 measurement Methods 0.000 description 1
239000000155 melt Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
229940066842 petrolatum Drugs 0.000 description 1
239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
229920000053 polysorbate 80 Polymers 0.000 description 1
230000035755 proliferation Effects 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
239000002002 slurry Substances 0.000 description 1
241000894007 species Species 0.000 description 1
230000001954 sterilising effect Effects 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000013589 supplement Substances 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
238000005303 weighing Methods 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
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- 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)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Carbon And Carbon Compounds (AREA)

NL8203767A 1981-09-29 1982-09-29 Carbonzuuramidothiolcarbamaatderivaten bevattend onkruidbestrijdingsmiddel en werkwijze voor de bereiding van de actieve stoffen. NL8203767A (nl)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
HU812794A HU183589B (en)	1981-09-29	1981-09-29	Herbicide composition containing carboxylic acid-amido-thiol-carbamate derivatives and process for preparing the active substances
HU279481		1981-09-29

Publications (1)

Publication Number	Publication Date
NL8203767A true NL8203767A (nl)	1983-04-18

Family

ID=10961120

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NL8203767A NL8203767A (nl)	1981-09-29	1982-09-29	Carbonzuuramidothiolcarbamaatderivaten bevattend onkruidbestrijdingsmiddel en werkwijze voor de bereiding van de actieve stoffen.

Country Status (21)

Country	Link
US (1)	US4559083A (fr)
AT (1)	AT381618B (fr)
BE (1)	BE894492A (fr)
BG (2)	BG40653A3 (fr)
CA (1)	CA1217766A (fr)
CH (1)	CH655305A5 (fr)
CS (1)	CS235963B2 (fr)
DD (2)	DD210260A5 (fr)
DE (1)	DE3236097A1 (fr)
DK (1)	DK430682A (fr)
FR (1)	FR2513485B1 (fr)
GB (1)	GB2106518B (fr)
GR (1)	GR77658B (fr)
HU (1)	HU183589B (fr)
IT (1)	IT1210938B (fr)
NL (1)	NL8203767A (fr)
PL (1)	PL135607B1 (fr)
PT (1)	PT75613B (fr)
RO (1)	RO88971A (fr)
SU (2)	SU1416045A3 (fr)
TR (1)	TR21704A (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5504109A (en) *	1989-05-13	1996-04-02	Bayer Aktiengesellschaft	Susbstituted amino acid amide derivatives their preparation and use
DE3915755A1 (de) *	1989-05-13	1990-11-29	Bayer Ag	Fungizide mittel sowie substituierte aminosaeureamid-derivate und deren herstellung
DE4203084A1 (de) *	1992-02-04	1993-08-05	Bayer Ag	Substituierte aminosaeureamide
CN102452959A (zh) *	2010-10-20	2012-05-16	中国农业科学院植物保护研究所	取代的缬氨酰胺衍生物及其制备
USD951590S1 (en) *	2019-12-16	2022-05-17	LaShonda Epps	Pocket bra

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4108885A (en) *	1967-08-25	1978-08-22	Schering Ag	Salts of thiocarbamic esters with fungicidal and fungistatic action
US3493360A (en) *	1968-05-14	1970-02-03	Stauffer Chemical Co	Herbicides
US3897474A (en) *	1972-10-12	1975-07-29	Ciba Geigy Corp	Thiol and dithiol carbamate acid ester derivatives of phenyl formamidine
JPS52153935A (en) *	1976-06-11	1977-12-21	Kyowa Hakko Kogyo Co Ltd	Novel sarocosine derivatives and herbicides containing same
JPS52151146A (en) *	1976-06-11	1977-12-15	Kyowa Hakko Kogyo Co Ltd	Novel thiocarbonylamino acid derivatives and novel herbicides containing same
JPS53148530A (en) *	1977-05-27	1978-12-25	Kyowa Hakko Kogyo Co Ltd	Agricultural and horticultural fungicide

1981
- 1981-09-29 HU HU812794A patent/HU183589B/hu unknown
1982
- 1982-09-22 US US06/421,238 patent/US4559083A/en not_active Expired - Fee Related
- 1982-09-22 AT AT0352182A patent/AT381618B/de not_active IP Right Cessation
- 1982-09-24 TR TR21704A patent/TR21704A/xx unknown
- 1982-09-27 DD DD82250403A patent/DD210260A5/de unknown
- 1982-09-27 BE BE1/10596A patent/BE894492A/fr not_active IP Right Cessation
- 1982-09-27 DD DD82243523A patent/DD204608A5/de unknown
- 1982-09-28 FR FR8216274A patent/FR2513485B1/fr not_active Expired
- 1982-09-28 SU SU823494193A patent/SU1416045A3/ru active
- 1982-09-28 GB GB08227657A patent/GB2106518B/en not_active Expired
- 1982-09-28 CH CH5695/82A patent/CH655305A5/de not_active IP Right Cessation
- 1982-09-28 CA CA000412374A patent/CA1217766A/fr not_active Expired
- 1982-09-28 DK DK430682A patent/DK430682A/da not_active Application Discontinuation
- 1982-09-28 GR GR69384A patent/GR77658B/el unknown
- 1982-09-28 PL PL1982238404A patent/PL135607B1/pl unknown
- 1982-09-28 IT IT8223463A patent/IT1210938B/it active
- 1982-09-28 PT PT75613A patent/PT75613B/pt unknown
- 1982-09-29 RO RO82113505A patent/RO88971A/fr unknown
- 1982-09-29 NL NL8203767A patent/NL8203767A/nl not_active Application Discontinuation
- 1982-09-29 BG BG059441A patent/BG40653A3/xx unknown
- 1982-09-29 BG BG058133A patent/BG40474A3/xx unknown
- 1982-09-29 CS CS826953A patent/CS235963B2/cs unknown
- 1982-09-29 DE DE19823236097 patent/DE3236097A1/de not_active Withdrawn
1983
- 1983-09-15 SU SU833642746A patent/SU1272979A3/ru active

Also Published As

Publication number	Publication date
BE894492A (fr)	1983-03-28
BG40474A3 (en)	1986-12-15
PL238404A1 (en)	1983-04-25
HU183589B (en)	1984-05-28
DK430682A (da)	1983-03-30
DD204608A5 (de)	1983-12-07
FR2513485B1 (fr)	1988-09-16
FR2513485A1 (fr)	1983-04-01
US4559083A (en)	1985-12-17
CH655305A5 (de)	1986-04-15
GB2106518A (en)	1983-04-13
BG40653A3 (en)	1986-01-15
SU1272979A3 (ru)	1986-11-23
PL135607B1 (en)	1985-11-30
TR21704A (tr)	1985-03-18
PT75613A (en)	1982-10-01
DE3236097A1 (de)	1983-04-14
ATA352182A (de)	1986-04-15
AT381618B (de)	1986-11-10
CA1217766A (fr)	1987-02-10
PT75613B (en)	1984-12-10
CS235963B2 (en)	1985-05-15
DD210260A5 (de)	1984-06-06
RO88971A (fr)	1986-04-30
IT1210938B (it)	1989-09-29
GB2106518B (en)	1985-07-17
GR77658B (fr)	1984-09-25
SU1416045A3 (ru)	1988-08-07
IT8223463A0 (it)	1982-09-28

Legal Events

Date	Code	Title
1983-07-01	BT	A notification was added to the application dossier and made available to the public
1985-01-01	A85	Still pending on 85-01-01
1989-05-01	BV	The patent application has lapsed

Publication	Publication Date	Title
NO143939B (no)	1981-02-02	Alfa-(4-(4`-trifluormetylfenoksy)-fenoksy)-propionsyrer og derivater herav for anvendelse som herbicider
JPH0228159A (ja)	1990-01-30	複素環式２―アルコキシフエノキシスルホニル尿素類、それらの製造方法およびそれらを含有する除草剤
US3953445A (en)	1976-04-27	3-Phenyl-6-halo-pyridazinyl thio-and dithio-carbonates
ITMI970554A1 (it)	1998-09-13	Amminosolfoniluree ad attivita' erbicida
CA2007351A1 (fr)	1990-07-11	Antidotes pour ameliorer la tolerance de plantes cultivees vis-a-vis de substances agrochimiques actives
NL8203767A (nl)	1983-04-18	Carbonzuuramidothiolcarbamaatderivaten bevattend onkruidbestrijdingsmiddel en werkwijze voor de bereiding van de actieve stoffen.
CS196220B2 (en)	1980-03-31	Fungicides and method of producing the active constituent
KR950005199B1 (ko)	1995-05-19	N'-치환된-n,n'-디아실히드라진의 6원 헤테로 고리 유도체
US4626273A (en)	1986-12-02	Herbicidal novel 2-alkoxyaminosulfonyl-benzene-sulfonylureas
US4210440A (en)	1980-07-01	Urea derivatives, process for preparing the same and herbicidal composition containing the same
CA1098531A (fr)	1981-03-31	Traduction non-disponible
PL120535B1 (en)	1982-03-31	Pesticide or plant growth regulator and process for manufacturing sulfonanilidesenijj i sposob poluchenija sul'fonanilidov
CS257781B2 (en)	1988-06-15	Agent for compensation of phytotoxical effects caused by herbicides and method of its antitoxic active substance production
CA1215553A (fr)	1986-12-23	Composes heterocycliques herbicides
JPH111473A (ja)	1999-01-06	除草活性を有するアリール複素環類
US5721192A (en)	1998-02-24	Aminosulfonyl ureas
CN105218517A (zh)	2016-01-06	N-(氰基环丙基)苯甲酰胺类化合物及其应用
JPS60146878A (ja)	1985-08-02	スルホニルグアニジン誘導体，その製法及び除草剤
KR950013855B1 (ko)	1995-11-17	제초제 활성이 있는 우레아 유도체와 그 제조방법
US5175289A (en)	1992-12-29	1,2,4-triazolo-[1,5a]pyrimidin-2-yl derivatives
NL8302514A (nl)	1984-02-01	Gesubstitueerde aceetamidederivaten met werking als antigif, antigifsamenstellingen bevattende dergelijke verbindingen, selectief-herbicidesamenstellingen bevattende deze antigiffen en een werkwijze voor de bereiding van gesubstitueerde aceetamidederivaten.
AU606474B2 (en)	1991-02-07	Furazanylureas
CN107915718B (zh)	2021-04-02	有杀虫活性的n-酰基烷基苯甲酰氨类化合物及其应用
KR810000603B1 (ko)	1981-06-05	N-(1, 3, 4-티아디아졸-2-일)벤즈아미드의 제조방법
KR820000804B1 (ko)	1982-05-11	페녹시-페녹시 프로피온산 유도체의 제조방법