IL44925A - N-cycloalkyl(norbornyl)thiolcarbamates their preparation and their use as herbicides - Google Patents
N-cycloalkyl(norbornyl)thiolcarbamates their preparation and their use as herbicidesInfo
- Publication number
- IL44925A IL44925A IL44925A IL4492574A IL44925A IL 44925 A IL44925 A IL 44925A IL 44925 A IL44925 A IL 44925A IL 4492574 A IL4492574 A IL 4492574A IL 44925 A IL44925 A IL 44925A
- Authority
- IL
- Israel
- Prior art keywords
- spp
- substituted
- denotes
- norbornyl
- thiol
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title abstract description 8
- 238000002360 preparation method Methods 0.000 title description 3
- 230000012010 growth Effects 0.000 claims abstract description 4
- 238000000034 method Methods 0.000 claims abstract 3
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- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 claims description 7
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- 241001520808 Panicum virgatum Species 0.000 description 1
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- 241000219833 Phaseolus Species 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
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- 241000209504 Poaceae Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
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- 241000208476 Primulaceae Species 0.000 description 1
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- 241000218201 Ranunculaceae Species 0.000 description 1
- 241000218206 Ranunculus Species 0.000 description 1
- 241000593769 Richardia <angiosperm> Species 0.000 description 1
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- 241000583552 Scleranthus annuus Species 0.000 description 1
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- 235000012308 Tagetes Nutrition 0.000 description 1
- 241000736851 Tagetes Species 0.000 description 1
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- 235000014787 Vitis vinifera Nutrition 0.000 description 1
- 241001506766 Xanthium Species 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 241000159213 Zygophyllaceae Species 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 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
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 150000001448 anilines Chemical class 0.000 description 1
- 239000000729 antidote Substances 0.000 description 1
- 229940075522 antidotes Drugs 0.000 description 1
- 229940111121 antirheumatic drug quinolines Drugs 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- BUSBFZWLPXDYIC-UHFFFAOYSA-N arsonic acid Chemical class O[AsH](O)=O BUSBFZWLPXDYIC-UHFFFAOYSA-N 0.000 description 1
- 244000030166 artemisia Species 0.000 description 1
- 235000009052 artemisia Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001556 benzimidazoles Chemical class 0.000 description 1
- 150000005130 benzoxazines Chemical class 0.000 description 1
- JEPPYVOSGKWVSJ-UHFFFAOYSA-N bicyclo[2.2.1]heptan-3-amine Chemical compound C1CC2C(N)CC1C2 JEPPYVOSGKWVSJ-UHFFFAOYSA-N 0.000 description 1
- 159000000007 calcium salts Chemical class 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- 239000001511 capsicum annuum Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 235000013339 cereals Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000011280 coal tar Substances 0.000 description 1
- 229940108066 coal tar Drugs 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- ZHHMZBGCUSMICG-UHFFFAOYSA-N diazinane-3-thione Chemical class S=C1CCCNN1 ZHHMZBGCUSMICG-UHFFFAOYSA-N 0.000 description 1
- 239000002283 diesel fuel Substances 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 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
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 241001233957 eudicotyledons Species 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000002532 grape seed extract Nutrition 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 150000001469 hydantoins Chemical class 0.000 description 1
- 150000002460 imidazoles Chemical class 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
- 239000003350 kerosene Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 210000001699 lower leg Anatomy 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound 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
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012074 organic phase Substances 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
- BRIPEFGONNNPNE-UHFFFAOYSA-N oxadiazolidine-4-thione Chemical class S=C1CONN1 BRIPEFGONNNPNE-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 150000002989 phenols Chemical class 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
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical class CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 150000004892 pyridazines Chemical class 0.000 description 1
- 150000003222 pyridines 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
- 150000003246 quinazolines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 150000004760 silicates Chemical class 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
- 238000009331 sowing Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
- 229960000278 theophylline Drugs 0.000 description 1
- OLPRIZQBWZMBAS-UHFFFAOYSA-N thiadiazolidine 1,1-dioxide Chemical class O=S1(=O)CCNN1 OLPRIZQBWZMBAS-UHFFFAOYSA-N 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
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/02—Monothiocarbamic acids; Derivatives thereof
- C07C333/06—Monothiocarbamic acids; Derivatives thereof having nitrogen atoms of thiocarbamic groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
- C07C2601/14—The ring being saturated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
- C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catching Or Destruction (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2329043A DE2329043A1 (de) | 1973-06-07 | 1973-06-07 | Carbothiolate |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL44925A0 IL44925A0 (en) | 1974-07-31 |
| IL44925A true IL44925A (en) | 1977-06-30 |
Family
ID=5883330
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL44925A IL44925A (en) | 1973-06-07 | 1974-05-30 | N-cycloalkyl(norbornyl)thiolcarbamates their preparation and their use as herbicides |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US3947485A (fr) |
| JP (1) | JPS5019928A (fr) |
| AR (1) | AR219893A1 (fr) |
| AT (1) | AT334678B (fr) |
| BE (1) | BE816074A (fr) |
| BG (1) | BG22812A3 (fr) |
| BR (1) | BR7404666D0 (fr) |
| CA (1) | CA1024159A (fr) |
| CH (1) | CH584506A5 (fr) |
| CS (1) | CS181760B2 (fr) |
| DD (1) | DD111636A5 (fr) |
| DE (1) | DE2329043A1 (fr) |
| DK (1) | DK140459C (fr) |
| EG (1) | EG11484A (fr) |
| ES (1) | ES427039A1 (fr) |
| FR (1) | FR2232543B1 (fr) |
| GB (1) | GB1463597A (fr) |
| HU (1) | HU169162B (fr) |
| IL (1) | IL44925A (fr) |
| IT (1) | IT1049289B (fr) |
| NL (1) | NL7407211A (fr) |
| PH (1) | PH10893A (fr) |
| SE (1) | SE408416B (fr) |
| SU (1) | SU522769A3 (fr) |
| ZA (1) | ZA743532B (fr) |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE571955A (fr) * | 1956-01-17 | |||
| US2916369A (en) * | 1956-09-26 | 1959-12-08 | Stauffer Chemical Co | Diallylthiolcarbamates and their use as herbicides |
| US2901498A (en) * | 1957-01-11 | 1959-08-25 | Stauffer Chemical Co | N-alkyl, n-allyl thiolcarbamate compositions |
| US2901499A (en) * | 1957-02-13 | 1959-08-25 | Stauffer Chemical Co | Lower alkyl esters of n-alkoxyalkylthiolcarbamic acids |
| US2916370A (en) * | 1957-04-02 | 1959-12-08 | Stauffer Chemical Co | Chlorinated thiolcarbamates and their use as herbicides |
| US3151119A (en) * | 1959-12-31 | 1964-09-29 | Monsanto Co | Method for preparing substituted thiolcarbamates |
| US3224863A (en) * | 1962-06-13 | 1965-12-21 | Monsanto Co | Vegetation control with unsaturated hydrocarbon esters of n,n-disubstituted thionocarbamic acids |
| US3264339A (en) * | 1964-05-05 | 1966-08-02 | Standard Oil Co | Process for the preparation of s-(2-hydroxyalkyl) and s-(2-mercaptoalkyl) esters |
-
1973
- 1973-06-07 DE DE2329043A patent/DE2329043A1/de active Pending
-
1974
- 1974-05-29 NL NL7407211A patent/NL7407211A/xx not_active Application Discontinuation
- 1974-05-30 IL IL44925A patent/IL44925A/en unknown
- 1974-05-31 CA CA201,377A patent/CA1024159A/fr not_active Expired
- 1974-05-31 AR AR254022A patent/AR219893A1/es active
- 1974-05-31 US US05/474,900 patent/US3947485A/en not_active Expired - Lifetime
- 1974-06-01 EG EG195/74A patent/EG11484A/xx active
- 1974-06-04 ZA ZA00743532A patent/ZA743532B/xx unknown
- 1974-06-05 IT IT51399/74A patent/IT1049289B/it active
- 1974-06-05 SE SE7407410A patent/SE408416B/xx unknown
- 1974-06-05 JP JP49062982A patent/JPS5019928A/ja active Pending
- 1974-06-05 DD DD178968A patent/DD111636A5/xx unknown
- 1974-06-06 GB GB2517774A patent/GB1463597A/en not_active Expired
- 1974-06-06 AT AT469974A patent/AT334678B/de not_active IP Right Cessation
- 1974-06-06 ES ES427039A patent/ES427039A1/es not_active Expired
- 1974-06-06 DK DK302874A patent/DK140459C/da active
- 1974-06-06 BR BR4666/74A patent/BR7404666D0/pt unknown
- 1974-06-06 BG BG26888A patent/BG22812A3/xx unknown
- 1974-06-06 SU SU2034994A patent/SU522769A3/ru active
- 1974-06-06 CS CS7400004034A patent/CS181760B2/cs unknown
- 1974-06-06 HU HUBA3084A patent/HU169162B/hu unknown
- 1974-06-07 FR FR7419776A patent/FR2232543B1/fr not_active Expired
- 1974-06-07 CH CH785674A patent/CH584506A5/xx not_active IP Right Cessation
- 1974-06-07 BE BE145209A patent/BE816074A/fr unknown
- 1974-06-07 PH PH15914A patent/PH10893A/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| IL44925A0 (en) | 1974-07-31 |
| ATA469974A (de) | 1976-05-15 |
| PH10893A (en) | 1977-09-30 |
| DK140459C (da) | 1980-02-04 |
| NL7407211A (fr) | 1974-12-10 |
| DK140459B (da) | 1979-09-03 |
| FR2232543B1 (fr) | 1977-09-30 |
| ZA743532B (en) | 1975-06-25 |
| AT334678B (de) | 1976-01-25 |
| BG22812A3 (fr) | 1977-04-20 |
| US3947485A (en) | 1976-03-30 |
| CS181760B2 (en) | 1978-03-31 |
| DE2329043A1 (de) | 1975-01-02 |
| SU522769A3 (ru) | 1976-07-25 |
| BE816074A (fr) | 1974-12-09 |
| DD111636A5 (fr) | 1975-03-05 |
| HU169162B (fr) | 1976-10-28 |
| GB1463597A (en) | 1977-02-02 |
| AR219893A1 (es) | 1980-09-30 |
| DK302874A (fr) | 1975-02-17 |
| ES427039A1 (es) | 1976-07-16 |
| SE7407410L (fr) | 1974-12-09 |
| BR7404666D0 (pt) | 1975-09-30 |
| FR2232543A1 (fr) | 1975-01-03 |
| CH584506A5 (fr) | 1977-02-15 |
| EG11484A (en) | 1978-03-29 |
| SE408416B (sv) | 1979-06-11 |
| IT1049289B (it) | 1981-01-20 |
| JPS5019928A (fr) | 1975-03-03 |
| CA1024159A (fr) | 1978-01-10 |
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