GB834358A - N-monoaryl substituted carbamic acid 2, 4, 5-trichlorophenyl esters - Google Patents
N-monoaryl substituted carbamic acid 2, 4, 5-trichlorophenyl estersInfo
- Publication number
- GB834358A GB834358A GB37504/57A GB3750457A GB834358A GB 834358 A GB834358 A GB 834358A GB 37504/57 A GB37504/57 A GB 37504/57A GB 3750457 A GB3750457 A GB 3750457A GB 834358 A GB834358 A GB 834358A
- Authority
- GB
- United Kingdom
- Prior art keywords
- prepared
- compound
- ester
- phenyl
- carbamic acid
- 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
- JMYRIUZLEQJWNF-UHFFFAOYSA-N (2,4,5-trichlorophenyl) carbamate Chemical class NC(=O)OC1=CC(Cl)=C(Cl)C=C1Cl JMYRIUZLEQJWNF-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 6
- 150000002148 esters Chemical class 0.000 abstract 6
- 239000000203 mixture Substances 0.000 abstract 6
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 4
- 239000000460 chlorine Chemical group 0.000 abstract 4
- 229910052801 chlorine Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 4
- 239000003973 paint Substances 0.000 abstract 4
- 241000233866 Fungi Species 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 239000000654 additive Substances 0.000 abstract 3
- -1 aromatic isocyanate Chemical class 0.000 abstract 3
- 239000003701 inert diluent Substances 0.000 abstract 3
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 239000005995 Aluminium silicate Substances 0.000 abstract 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract 2
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract 2
- 239000002202 Polyethylene glycol Substances 0.000 abstract 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 2
- 239000004480 active ingredient Substances 0.000 abstract 2
- 230000000996 additive effect Effects 0.000 abstract 2
- 235000012211 aluminium silicate Nutrition 0.000 abstract 2
- 150000004982 aromatic amines Chemical class 0.000 abstract 2
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- 239000000839 emulsion Substances 0.000 abstract 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 abstract 2
- YSBUANSGDLZTKV-UHFFFAOYSA-N n-phenylcarbamoyl chloride Chemical compound ClC(=O)NC1=CC=CC=C1 YSBUANSGDLZTKV-UHFFFAOYSA-N 0.000 abstract 2
- 229920001223 polyethylene glycol Polymers 0.000 abstract 2
- 239000000843 powder Substances 0.000 abstract 2
- UGLCEIWDYLOYCE-UHFFFAOYSA-N (2,4,5-trichlorophenyl) N-(4-methylphenyl)carbamate Chemical compound ClC1=C(C=C(C(=C1)Cl)Cl)OC(NC1=CC=C(C=C1)C)=O UGLCEIWDYLOYCE-UHFFFAOYSA-N 0.000 abstract 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000000443 aerosol Substances 0.000 abstract 1
- 238000007605 air drying Methods 0.000 abstract 1
- 229920000180 alkyd Polymers 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 239000001273 butane Substances 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000004651 carbonic acid esters Chemical class 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- AOGYCOYQMAVAFD-UHFFFAOYSA-N chlorocarbonic acid Chemical compound OC(Cl)=O AOGYCOYQMAVAFD-UHFFFAOYSA-N 0.000 abstract 1
- 239000012141 concentrate Substances 0.000 abstract 1
- 239000002781 deodorant agent Substances 0.000 abstract 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 abstract 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- 238000010790 dilution Methods 0.000 abstract 1
- 239000012895 dilution Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 239000000945 filler Substances 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 239000012948 isocyanate Substances 0.000 abstract 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 abstract 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 abstract 1
- 229940049964 oleate Drugs 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 abstract 1
- PWXJULSLLONQHY-UHFFFAOYSA-N phenylcarbamic acid Chemical compound OC(=O)NC1=CC=CC=C1 PWXJULSLLONQHY-UHFFFAOYSA-N 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 239000000344 soap Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 abstract 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 239000008096 xylene Substances 0.000 abstract 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (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 |
|---|---|---|---|
| DE359562X | 1956-12-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB834358A true GB834358A (en) | 1960-05-04 |
Family
ID=6291219
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB37504/57A Expired GB834358A (en) | 1956-12-04 | 1957-12-02 | N-monoaryl substituted carbamic acid 2, 4, 5-trichlorophenyl esters |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE562631A (enrdf_load_stackoverflow) |
| CH (1) | CH359562A (enrdf_load_stackoverflow) |
| DE (1) | DE1020971B (enrdf_load_stackoverflow) |
| GB (1) | GB834358A (enrdf_load_stackoverflow) |
| NL (2) | NL222578A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2138804A (en) * | 1983-04-27 | 1984-10-31 | Sumitomo Chemical Co | Fungicidal N-phenylcarbamates |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1166180B (de) * | 1960-06-07 | 1964-03-26 | Bayer Ag | Verfahren zur Herstellung von Carbaminsaeureestern |
| FR2614300A1 (fr) * | 1987-04-22 | 1988-10-28 | Sanofi Sa | Nouveau procede d'obtention de carbamates actives. |
-
0
- NL NL99972D patent/NL99972C/xx active
- NL NL222578D patent/NL222578A/xx unknown
- BE BE562631D patent/BE562631A/xx unknown
- DE DENDAT1020971D patent/DE1020971B/de active Pending
-
1957
- 1957-11-21 CH CH359562D patent/CH359562A/de unknown
- 1957-12-02 GB GB37504/57A patent/GB834358A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2138804A (en) * | 1983-04-27 | 1984-10-31 | Sumitomo Chemical Co | Fungicidal N-phenylcarbamates |
Also Published As
| Publication number | Publication date |
|---|---|
| NL222578A (enrdf_load_stackoverflow) | |
| NL99972C (enrdf_load_stackoverflow) | |
| CH359562A (de) | 1962-01-15 |
| DE1020971B (de) | 1957-12-19 |
| BE562631A (enrdf_load_stackoverflow) |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3063823A (en) | Method of killing weeds and influencing plant growth | |
| US2788268A (en) | Novel compositions and their use | |
| US3501578A (en) | Fungicidal composition containing phenyl - mercaptomethane-sulfonamide and method of using the same | |
| GB743958A (en) | Improvements in or relating to pesticides | |
| GB834358A (en) | N-monoaryl substituted carbamic acid 2, 4, 5-trichlorophenyl esters | |
| US3492333A (en) | Carbamidoximes | |
| US2951786A (en) | Bactericidal and fungicidal compositions comprising pentahalophenyl n-(phenyl) carbamates | |
| GB984514A (en) | Protection of organic materials against attack by fungi or bacteria | |
| CA1153013A (en) | Process for the preparation of new sulphonic acid cycloalkylamides and their use as microbicides | |
| FI73422C (fi) | 1-(trihalogenmetylsulfenyl)-4-aryl-1, 2,4-triazolidin-5-oner, och dessa innehaollande fungicider och foerfarande foer bekaempning av svampar med dem. | |
| US3816532A (en) | Ketoxime carbamate pesticides | |
| US4257803A (en) | Diurethanes and methods for their use in herbicidal compositions | |
| US3491109A (en) | 3,5-dioxo-1,2,4-thiadiazolidines | |
| US3504091A (en) | Method of combatting fungi with n,n dialkyl substituted dithiocyanoanilines | |
| US2936262A (en) | Diels-alder adduct of tetrachloro cyclopentadiene with quinone as a fungicide | |
| HU188735B (en) | Fungicide compositions containing n-sulphenylated buiret derivatives process for preparing the compounds | |
| US4185989A (en) | 3-Phenacyl phthaldide safening agents | |
| US3376335A (en) | Carbamic acid esters | |
| US3636001A (en) | Amine salts of nitraminotriazoles | |
| US2553774A (en) | N-thiotrichloromethyl morpholine and fungicidal compositions containing same | |
| US3629252A (en) | 3-arylimino-4-chloro-5-amino-1 2-dithiols | |
| US2300611A (en) | Stabilized insecticides | |
| US3472936A (en) | Synergistic fungicidal composition | |
| ES329012A1 (es) | Un procedimiento para la preparacion de benzimidazolas sus-tituidas. | |
| AT364671B (de) | Insektizides mittel |