SU1210650A3 - Гербицидное средство (его варианты) - Google Patents
Гербицидное средство (его варианты) Download PDFInfo
- Publication number
- SU1210650A3 SU1210650A3 SU802900896A SU2900896A SU1210650A3 SU 1210650 A3 SU1210650 A3 SU 1210650A3 SU 802900896 A SU802900896 A SU 802900896A SU 2900896 A SU2900896 A SU 2900896A SU 1210650 A3 SU1210650 A3 SU 1210650A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- text
- sup
- sub
- hydrogen
- methyl
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title claims description 9
- 230000002363 herbicidal effect Effects 0.000 title claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- 239000000460 chlorine Chemical group 0.000 claims abstract description 6
- 229910052801 chlorine Chemical group 0.000 claims abstract description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 12
- 239000013543 active substance Substances 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 8
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims description 6
- 239000004563 wettable powder Substances 0.000 claims description 5
- 239000005639 Lauric acid Substances 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 239000007859 condensation product Substances 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical class OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 claims description 3
- 239000013589 supplement Substances 0.000 claims description 3
- 125000006022 2-methyl-2-propenyl group Chemical group 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 230000005494 condensation Effects 0.000 claims description 2
- 238000009833 condensation Methods 0.000 claims description 2
- 150000002148 esters Chemical class 0.000 claims description 2
- 239000008096 xylene Substances 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229920002678 cellulose Polymers 0.000 claims 1
- 239000001913 cellulose Substances 0.000 claims 1
- 239000000047 product Substances 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract description 9
- 241000196324 Embryophyta Species 0.000 abstract description 6
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- -1 carbanilic acid ester Chemical class 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical group 0.000 abstract 2
- 235000007319 Avena orientalis Nutrition 0.000 abstract 1
- 244000075850 Avena orientalis Species 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 240000005979 Hordeum vulgare Species 0.000 abstract 1
- 235000007340 Hordeum vulgare Nutrition 0.000 abstract 1
- 240000007594 Oryza sativa Species 0.000 abstract 1
- 235000007164 Oryza sativa Nutrition 0.000 abstract 1
- 241000209504 Poaceae Species 0.000 abstract 1
- 241000209056 Secale Species 0.000 abstract 1
- 235000007238 Secale cereale Nutrition 0.000 abstract 1
- 241000209140 Triticum Species 0.000 abstract 1
- 235000021307 Triticum Nutrition 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 235000009566 rice Nutrition 0.000 abstract 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 229940126062 Compound A Drugs 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- WOZQBERUBLYCEG-UHFFFAOYSA-N SWEP Chemical compound COC(=O)NC1=CC=C(Cl)C(Cl)=C1 WOZQBERUBLYCEG-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- HZVVJJIYJKGMFL-UHFFFAOYSA-N almasilate Chemical compound O.[Mg+2].[Al+3].[Al+3].O[Si](O)=O.O[Si](O)=O HZVVJJIYJKGMFL-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 230000005080 plant death 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
- 239000000126 substance Substances 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 230000004580 weight loss Effects 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
- A01N47/20—N-Aryl derivatives 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)
- Indole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792913976 DE2913976A1 (de) | 1979-04-05 | 1979-04-05 | Substituierte carbanilsaeureester, verfahren zur herstellung dieser verbindungen sowie diese enthaltende selektive herbizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU1210650A3 true SU1210650A3 (ru) | 1986-02-07 |
Family
ID=6067687
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU802900896A SU1210650A3 (ru) | 1979-04-05 | 1980-04-01 | Гербицидное средство (его варианты) |
| SU802901455A SU1048983A3 (ru) | 1979-04-05 | 1980-04-01 | Способ получени замещенных сложных эфиров карбаниловой кислоты |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU802901455A SU1048983A3 (ru) | 1979-04-05 | 1980-04-01 | Способ получени замещенных сложных эфиров карбаниловой кислоты |
Country Status (38)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6070775U (ja) * | 1983-10-21 | 1985-05-18 | ヤンマーディーゼル株式会社 | 横形内燃機関の燃料浄化装置 |
| FR2662159B1 (fr) * | 1990-05-15 | 1994-03-11 | Matieres Nucleaires Cie Gle | Nouveaux ligands thio-ethers et leur utilisation pour separer le palladium de solutions aqueuses, en particulier de soludtions nitriques de dissolution d'elements combustibles nucleaires irradies. |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL273837A (enExample) | 1961-01-25 | |||
| US4093447A (en) * | 1971-06-23 | 1978-06-06 | Bayer Aktiengesellschaft | N-Arylcarbamic acid esters and plant growth regulant compositions and methods |
| DE2417487C2 (de) * | 1974-04-10 | 1983-01-20 | Hoechst Ag, 6000 Frankfurt | Benzyl-phenoxyalkancarbonsäuren, deren Derivate und Verfahren zu ihrer Herstellung |
| US4149874A (en) * | 1977-06-21 | 1979-04-17 | Stauffer Chemical Company | Substituted cyclopropylmethoxy anilides and their use as herbicides |
| US4230483A (en) * | 1977-06-21 | 1980-10-28 | Stauffer Chemical Company | Substituted cyclopropylmethoxy phenyl carbamates and thiocarbamates and their use as herbicides |
| DE2804739A1 (de) * | 1978-02-02 | 1979-08-09 | Schering Ag | Phenylharnstoff-derivate, verfahren zur herstellung dieser verbindungen sowie diese enthaltendes selektives herbizides mittel |
-
1979
- 1979-04-05 DE DE19792913976 patent/DE2913976A1/de not_active Withdrawn
-
1980
- 1980-03-25 NL NL8001747A patent/NL8001747A/nl not_active Application Discontinuation
- 1980-03-26 CH CH238380A patent/CH646142A5/de not_active IP Right Cessation
- 1980-03-28 NZ NZ193299A patent/NZ193299A/xx unknown
- 1980-03-31 IL IL59738A patent/IL59738A/xx unknown
- 1980-04-01 SU SU802900896A patent/SU1210650A3/ru active
- 1980-04-01 BR BR8002002A patent/BR8002002A/pt unknown
- 1980-04-01 IT IT21093/80A patent/IT1148777B/it active
- 1980-04-01 DD DD80220133A patent/DD151041A5/de unknown
- 1980-04-01 SE SE8002506A patent/SE8002506L/ not_active Application Discontinuation
- 1980-04-01 NO NO800945A patent/NO151284C/no unknown
- 1980-04-01 SU SU802901455A patent/SU1048983A3/ru active
- 1980-04-02 DK DK146580A patent/DK146580A/da not_active IP Right Cessation
- 1980-04-02 YU YU00908/80A patent/YU90880A/xx unknown
- 1980-04-02 MX MX808737U patent/MX6140E/es unknown
- 1980-04-02 AT AT0180880A patent/AT379289B/de not_active IP Right Cessation
- 1980-04-02 BG BG047215A patent/BG31474A3/xx unknown
- 1980-04-02 GR GR61613A patent/GR66674B/el unknown
- 1980-04-02 ES ES490257A patent/ES490257A0/es active Granted
- 1980-04-03 CA CA000349209A patent/CA1142535A/en not_active Expired
- 1980-04-03 AU AU57154/80A patent/AU531347B2/en not_active Ceased
- 1980-04-03 HU HU80820A patent/HU182605B/hu unknown
- 1980-04-03 LU LU82325A patent/LU82325A1/de unknown
- 1980-04-03 GB GB8011331A patent/GB2049674B/en not_active Expired
- 1980-04-03 IE IE679/80A patent/IE49660B1/en unknown
- 1980-04-03 ZA ZA00802034A patent/ZA802034B/xx unknown
- 1980-04-03 TR TR20607A patent/TR20607A/xx unknown
- 1980-04-03 PL PL1980223232A patent/PL121299B1/pl unknown
- 1980-04-03 PT PT71059A patent/PT71059A/pt unknown
- 1980-04-03 BE BE0/200116A patent/BE882631A/fr not_active IP Right Cessation
- 1980-04-03 IN IN244/DEL/80A patent/IN154063B/en unknown
- 1980-04-04 JP JP55043645A patent/JPS5825659B2/ja not_active Expired
- 1980-04-04 CS CS807124A patent/CS214828B2/cs unknown
- 1980-04-04 FR FR8007672A patent/FR2453141A1/fr active Granted
- 1980-04-04 MA MA18999A patent/MA18804A1/fr unknown
- 1980-04-04 CS CS802363A patent/CS214827B2/cs unknown
- 1980-04-04 RO RO80100725A patent/RO79224A/ro unknown
- 1980-04-05 EG EG208/80A patent/EG14377A/xx active
- 1980-04-07 PH PH23862A patent/PH15714A/en unknown
-
1982
- 1982-08-10 US US06/406,897 patent/US4479822A/en not_active Expired - Fee Related
Non-Patent Citations (1)
| Title |
|---|
| Патент DE № 1195549, кл. 45 19/02, опублик. 1966. * |
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