GB912895A - New substituted carbamates - Google Patents
New substituted carbamatesInfo
- Publication number
- GB912895A GB912895A GB4185160A GB4185160A GB912895A GB 912895 A GB912895 A GB 912895A GB 4185160 A GB4185160 A GB 4185160A GB 4185160 A GB4185160 A GB 4185160A GB 912895 A GB912895 A GB 912895A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- carbamate
- phenyl
- dimethyl
- compounds
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 150000004657 carbamic acid derivatives Chemical class 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 5
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 150000002989 phenols Chemical class 0.000 abstract 4
- -1 aryl carbamates Chemical class 0.000 abstract 3
- 235000010290 biphenyl Nutrition 0.000 abstract 3
- 239000004305 biphenyl Substances 0.000 abstract 3
- 125000006267 biphenyl group Chemical group 0.000 abstract 3
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 150000002148 esters Chemical class 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 239000007788 liquid Substances 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 150000002790 naphthalenes Chemical class 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- WNNZAHBBDIVWBB-UHFFFAOYSA-N (4-methylsulfanylphenyl) carbamate Chemical compound CSC1=CC=C(OC(N)=O)C=C1 WNNZAHBBDIVWBB-UHFFFAOYSA-N 0.000 abstract 1
- KGPGKOSHODHUSR-UHFFFAOYSA-N 3-methyl-4-methylsulfonylphenol Chemical compound CC1=CC(O)=CC=C1S(C)(=O)=O KGPGKOSHODHUSR-UHFFFAOYSA-N 0.000 abstract 1
- QASBCTGZKABPKX-UHFFFAOYSA-N 4-(methylsulfanyl)phenol Chemical compound CSC1=CC=C(O)C=C1 QASBCTGZKABPKX-UHFFFAOYSA-N 0.000 abstract 1
- ZCQSJUGIZGMDDA-UHFFFAOYSA-N 4-(methylsulfinyl)phenol Chemical compound CS(=O)C1=CC=C(O)C=C1 ZCQSJUGIZGMDDA-UHFFFAOYSA-N 0.000 abstract 1
- 241000238876 Acari Species 0.000 abstract 1
- 241001124076 Aphididae Species 0.000 abstract 1
- LHHPJUQBKLEFBF-UHFFFAOYSA-N CSC1=CC=C(N(C)C(O)=O)C=C1C Chemical compound CSC1=CC=C(N(C)C(O)=O)C=C1C LHHPJUQBKLEFBF-UHFFFAOYSA-N 0.000 abstract 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 abstract 1
- 241000256113 Culicidae Species 0.000 abstract 1
- 241000255925 Diptera Species 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- FUMJEKDBXCJRCT-UHFFFAOYSA-N O-(4-methyl-2-sulfanylphenyl) carbamothioate Chemical compound C(N)(OC1=C(C=C(C=C1)C)S)=S FUMJEKDBXCJRCT-UHFFFAOYSA-N 0.000 abstract 1
- 241001325166 Phacelia congesta Species 0.000 abstract 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 230000000895 acaricidal effect Effects 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000000440 bentonite Substances 0.000 abstract 1
- 229910000278 bentonite Inorganic materials 0.000 abstract 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 abstract 1
- NBYQXBYMEUOBON-UHFFFAOYSA-N carbamothioyl chloride Chemical class NC(Cl)=S NBYQXBYMEUOBON-UHFFFAOYSA-N 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 239000003337 fertilizer Substances 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- 150000002513 isocyanates Chemical class 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- 150000003141 primary amines Chemical class 0.000 abstract 1
- 150000003335 secondary amines Chemical class 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- NONOKGVFTBWRLD-UHFFFAOYSA-N thioisocyanate group Chemical group S(N=C=O)N=C=O NONOKGVFTBWRLD-UHFFFAOYSA-N 0.000 abstract 1
- ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 abstract 1
- 231100000331 toxic Toxicity 0.000 abstract 1
- 230000002588 toxic effect Effects 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEF30015A DE1162352B (de) | 1959-12-05 | 1959-12-05 | Verfahren zur Herstellung von Carbaminsaeureestern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB912895A true GB912895A (en) | 1962-12-12 |
Family
ID=7093564
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4185160A Expired GB912895A (en) | 1959-12-05 | 1960-12-05 | New substituted carbamates |
Country Status (6)
| Country | Link |
|---|---|
| BE (1) | BE597806A (enrdf_load_stackoverflow) |
| BR (1) | BR6024675D0 (enrdf_load_stackoverflow) |
| CH (1) | CH389314A (enrdf_load_stackoverflow) |
| DE (1) | DE1162352B (enrdf_load_stackoverflow) |
| GB (1) | GB912895A (enrdf_load_stackoverflow) |
| NL (2) | NL258661A (enrdf_load_stackoverflow) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3313684A (en) * | 1959-12-05 | 1967-04-11 | Bayer Ag | 3, 5-dimethyl-4-methylmercaptophenyl n-methyl carbamate and methods for combating insects |
| US3331894A (en) * | 1963-03-04 | 1967-07-18 | Hooker Chemical Corp | o-(diloweralkoxythiophosphinylthioalkyl)phenyl n-loweralkyl carbamates |
| US3349115A (en) * | 1963-02-19 | 1967-10-24 | Hooker Chemical Corp | Sulfur-containing carbamate insecticides |
| US3349116A (en) * | 1963-02-20 | 1967-10-24 | Hooker Chemical Corp | Ortho hydrocarbyloxy alkenylenephenyl nu-lower alkylcarbamates |
| US3419663A (en) * | 1963-03-04 | 1968-12-31 | Hooker Chemical Corp | Method for the control of insects using thioalkylphenyl carbamates |
| US3437684A (en) * | 1964-07-04 | 1969-04-08 | Bayer Ag | 3,5-dimethyl-4-alpha-allyl mercaptophenyl-n-methyl carbamic acid ester |
| US3470236A (en) * | 1964-06-27 | 1969-09-30 | Bayer Ag | Phenyl-n-methyl carbamic acid esters |
| FR2208890A1 (enrdf_load_stackoverflow) * | 1972-12-01 | 1974-06-28 | Bayer Ag | |
| WO2002053529A1 (en) * | 2000-12-29 | 2002-07-11 | 3M Innovative Properties Company | High-boiling electrolyte solvent |
| US7060692B2 (en) | 2000-08-31 | 2006-06-13 | Bayer Cropscience Ag | Active ingredient combinations comprising insecticidal and acaricidal properties |
| US8846567B2 (en) | 2009-03-25 | 2014-09-30 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19953775A1 (de) | 1999-11-09 | 2001-05-10 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE10015310A1 (de) | 2000-03-28 | 2001-10-04 | Bayer Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| DE102007045955A1 (de) | 2007-09-26 | 2009-04-09 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| EP2127522A1 (de) | 2008-05-29 | 2009-12-02 | Bayer CropScience AG | Wirkstoffkombinationen mit insektiziden und akariziden Eigenschaften |
| EP2227951A1 (de) | 2009-01-23 | 2010-09-15 | Bayer CropScience AG | Verwendung von Enaminocarbonylverbindungen zur Bekämpfung von durch Insekten übertragenen Viren |
| ES2527833T3 (es) | 2009-03-25 | 2015-01-30 | Bayer Cropscience Ag | Combinaciones de principios activos nematicidas que comprenden fluopiram y otro principio activo |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE529434A (enrdf_load_stackoverflow) * | 1953-06-09 |
-
0
- NL NL131470D patent/NL131470C/xx active
- NL NL258661D patent/NL258661A/xx unknown
- BE BE597806D patent/BE597806A/xx unknown
-
1959
- 1959-12-05 DE DEF30015A patent/DE1162352B/de active Pending
-
1960
- 1960-11-28 CH CH1329960A patent/CH389314A/de unknown
- 1960-12-02 BR BR12467560A patent/BR6024675D0/pt unknown
- 1960-12-05 GB GB4185160A patent/GB912895A/en not_active Expired
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3313684A (en) * | 1959-12-05 | 1967-04-11 | Bayer Ag | 3, 5-dimethyl-4-methylmercaptophenyl n-methyl carbamate and methods for combating insects |
| US3349115A (en) * | 1963-02-19 | 1967-10-24 | Hooker Chemical Corp | Sulfur-containing carbamate insecticides |
| US3349116A (en) * | 1963-02-20 | 1967-10-24 | Hooker Chemical Corp | Ortho hydrocarbyloxy alkenylenephenyl nu-lower alkylcarbamates |
| US3331894A (en) * | 1963-03-04 | 1967-07-18 | Hooker Chemical Corp | o-(diloweralkoxythiophosphinylthioalkyl)phenyl n-loweralkyl carbamates |
| US3419663A (en) * | 1963-03-04 | 1968-12-31 | Hooker Chemical Corp | Method for the control of insects using thioalkylphenyl carbamates |
| US3470236A (en) * | 1964-06-27 | 1969-09-30 | Bayer Ag | Phenyl-n-methyl carbamic acid esters |
| US3437684A (en) * | 1964-07-04 | 1969-04-08 | Bayer Ag | 3,5-dimethyl-4-alpha-allyl mercaptophenyl-n-methyl carbamic acid ester |
| FR2208890A1 (enrdf_load_stackoverflow) * | 1972-12-01 | 1974-06-28 | Bayer Ag | |
| US7060692B2 (en) | 2000-08-31 | 2006-06-13 | Bayer Cropscience Ag | Active ingredient combinations comprising insecticidal and acaricidal properties |
| WO2002053529A1 (en) * | 2000-12-29 | 2002-07-11 | 3M Innovative Properties Company | High-boiling electrolyte solvent |
| US6534220B2 (en) | 2000-12-29 | 2003-03-18 | 3M Innovative Properties Company | High-boiling electrolyte solvent |
| US8846567B2 (en) | 2009-03-25 | 2014-09-30 | Bayer Cropscience Ag | Active compound combinations having insecticidal and acaricidal properties |
Also Published As
| Publication number | Publication date |
|---|---|
| CH389314A (de) | 1965-03-15 |
| NL131470C (enrdf_load_stackoverflow) | |
| BR6024675D0 (pt) | 1973-06-12 |
| NL258661A (enrdf_load_stackoverflow) | |
| DE1162352B (de) | 1964-02-06 |
| BE597806A (enrdf_load_stackoverflow) |
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