CH619928A5 - - Google Patents
Download PDFInfo
- Publication number
- CH619928A5 CH619928A5 CH1505776A CH1505776A CH619928A5 CH 619928 A5 CH619928 A5 CH 619928A5 CH 1505776 A CH1505776 A CH 1505776A CH 1505776 A CH1505776 A CH 1505776A CH 619928 A5 CH619928 A5 CH 619928A5
- Authority
- CH
- Switzerland
- Prior art keywords
- fluoride
- methylcarbamoyl
- mol
- added
- alkyl
- Prior art date
Links
- -1 N- (N'-2-methoxyethoxycarbonyl-N'-methylaminosulfenyl) -N-methylcarbamoyl Chemical group 0.000 claims description 44
- 150000001875 compounds Chemical class 0.000 claims description 15
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 238000002360 preparation method Methods 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 9
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 125000002723 alicyclic group Chemical group 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 2
- 125000001326 naphthylalkyl group Chemical group 0.000 claims description 2
- 150000002825 nitriles Chemical class 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- 125000004434 sulfur atom Chemical group 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 1
- 239000010931 gold Substances 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 108
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 57
- 239000000243 solution Substances 0.000 description 39
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 37
- 238000003756 stirring Methods 0.000 description 23
- 239000000203 mixture Substances 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 22
- 238000006243 chemical reaction Methods 0.000 description 17
- 239000012299 nitrogen atmosphere Substances 0.000 description 17
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 16
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 14
- 239000000706 filtrate Substances 0.000 description 13
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 12
- 239000004698 Polyethylene Substances 0.000 description 9
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 9
- 239000012074 organic phase Substances 0.000 description 9
- 229920000573 polyethylene Polymers 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 229920006395 saturated elastomer Polymers 0.000 description 9
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 9
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 8
- 230000007935 neutral effect Effects 0.000 description 8
- 238000009835 boiling Methods 0.000 description 7
- 238000004821 distillation Methods 0.000 description 7
- 235000017557 sodium bicarbonate Nutrition 0.000 description 6
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 3
- 238000000605 extraction Methods 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- XYYUZKKOTPEAGC-UHFFFAOYSA-N 2-ethylhexyl n-chlorosulfanyl-n-methylcarbamate Chemical compound CCCCC(CC)COC(=O)N(C)SCl XYYUZKKOTPEAGC-UHFFFAOYSA-N 0.000 description 2
- PPQPHHZRIJJIPB-UHFFFAOYSA-N 2-methoxyethyl n-chlorosulfanyl-n-methylcarbamate Chemical compound COCCOC(=O)N(C)SCl PPQPHHZRIJJIPB-UHFFFAOYSA-N 0.000 description 2
- UEHCAXCOGBVFQF-UHFFFAOYSA-N CCCCCCOC([S+](N(C)CC)N(C)C(F)=O)=O Chemical compound CCCCCCOC([S+](N(C)CC)N(C)C(F)=O)=O UEHCAXCOGBVFQF-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- HNIKQHBIMQOXCQ-UHFFFAOYSA-N benzyl n-[carbonofluoridoyl(methyl)amino]sulfanyl-n-methylcarbamate Chemical compound FC(=O)N(C)SN(C)C(=O)OCC1=CC=CC=C1 HNIKQHBIMQOXCQ-UHFFFAOYSA-N 0.000 description 2
- SJMGTEDVEITXQR-UHFFFAOYSA-N butyl n-chlorosulfanyl-n-methylcarbamate Chemical compound CCCCOC(=O)N(C)SCl SJMGTEDVEITXQR-UHFFFAOYSA-N 0.000 description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 239000012442 inert solvent Substances 0.000 description 2
- JPSHMDUAFDEKAR-UHFFFAOYSA-N n-(1,4-dithian-2-ylidene)hydroxylamine Chemical compound ON=C1CSCCS1 JPSHMDUAFDEKAR-UHFFFAOYSA-N 0.000 description 2
- 150000002923 oximes Chemical class 0.000 description 2
- 239000012047 saturated solution Substances 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- FCMAPQSYNWNJDH-UHFFFAOYSA-N tert-butyl n-chlorosulfanyl-n-methylcarbamate Chemical compound ClSN(C)C(=O)OC(C)(C)C FCMAPQSYNWNJDH-UHFFFAOYSA-N 0.000 description 2
- KXRBRBHOAQYNKB-UHFFFAOYSA-N (4-chlorophenyl)methyl n-[carbonofluoridoyl(methyl)amino]sulfanyl-n-methylcarbamate Chemical compound FC(=O)N(C)SN(C)C(=O)OCC1=CC=C(Cl)C=C1 KXRBRBHOAQYNKB-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 1
- YIWOUOPMSLSOMG-UHFFFAOYSA-N 1-methoxypropan-2-yl n-methylcarbamate Chemical compound CNC(=O)OC(C)COC YIWOUOPMSLSOMG-UHFFFAOYSA-N 0.000 description 1
- CFMNRUWDFGHSBD-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethyl n-methylcarbamate Chemical compound CNC(=O)OCCOCCOC CFMNRUWDFGHSBD-UHFFFAOYSA-N 0.000 description 1
- NWIYTMPUEWIYLZ-UHFFFAOYSA-N 2-ethylhexyl n-methylcarbamate Chemical compound CCCCC(CC)COC(=O)NC NWIYTMPUEWIYLZ-UHFFFAOYSA-N 0.000 description 1
- UEEHLSVIWJCQCH-UHFFFAOYSA-N 2-methoxyethyl n-[carbonofluoridoyl(methyl)amino]sulfanyl-n-methylcarbamate Chemical compound COCCOC(=O)N(C)SN(C)C(F)=O UEEHLSVIWJCQCH-UHFFFAOYSA-N 0.000 description 1
- HZATZLOLZWIRDN-UHFFFAOYSA-N 2-methoxyethyl n-methylcarbamate Chemical compound CNC(=O)OCCOC HZATZLOLZWIRDN-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 241000208818 Helianthus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 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 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- QMDPEBMTDBSGAE-UHFFFAOYSA-N benzyl n-methylcarbamate Chemical compound CNC(=O)OCC1=CC=CC=C1 QMDPEBMTDBSGAE-UHFFFAOYSA-N 0.000 description 1
- YAUWHXKOYHADTR-UHFFFAOYSA-N butyl n-methylcarbamate Chemical compound CCCCOC(=O)NC YAUWHXKOYHADTR-UHFFFAOYSA-N 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- OGKJRDFTMDZVQR-UHFFFAOYSA-N chlorocarbamothioic s-acid Chemical compound OC(=S)NCl OGKJRDFTMDZVQR-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000012973 diazabicyclooctane Substances 0.000 description 1
- LOZWAPSEEHRYPG-UHFFFAOYSA-N dithiane Natural products C1CSCCS1 LOZWAPSEEHRYPG-UHFFFAOYSA-N 0.000 description 1
- KVXWVVKPQBMKJU-UHFFFAOYSA-N dodecyl n-[carbonofluoridoyl(methyl)amino]sulfanyl-n-methylcarbamate Chemical compound CCCCCCCCCCCCOC(=O)N(C)SN(C)C(F)=O KVXWVVKPQBMKJU-UHFFFAOYSA-N 0.000 description 1
- SBBJXSDFMNOWPO-UHFFFAOYSA-N dodecyl n-chlorosulfanyl-n-methylcarbamate Chemical compound CCCCCCCCCCCCOC(=O)N(C)SCl SBBJXSDFMNOWPO-UHFFFAOYSA-N 0.000 description 1
- KAMQYCQIVWNZRB-UHFFFAOYSA-N dodecyl n-methylcarbamate Chemical compound CCCCCCCCCCCCOC(=O)NC KAMQYCQIVWNZRB-UHFFFAOYSA-N 0.000 description 1
- OQCIDFLHUCWGOE-UHFFFAOYSA-N ethyl n-[carbonofluoridoyl(methyl)amino]sulfanyl-n-methylcarbamate Chemical compound CCOC(=O)N(C)SN(C)C(F)=O OQCIDFLHUCWGOE-UHFFFAOYSA-N 0.000 description 1
- YXXJYJNWSUUFBB-UHFFFAOYSA-N ethyl n-methylcarbamate Chemical compound [CH2]COC(=O)NC YXXJYJNWSUUFBB-UHFFFAOYSA-N 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000005646 oximino group Chemical group 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- JHLVEBNWCCKSGY-UHFFFAOYSA-N tert-butyl n-methylcarbamate Chemical compound CNC(=O)OC(C)(C)C JHLVEBNWCCKSGY-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/06—Compounds containing sulfur atoms only bound to two nitrogen atoms
- C07C381/08—Compounds containing sulfur atoms only bound to two nitrogen atoms having at least one of the nitrogen atoms acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C381/00—Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00
- C07C381/06—Compounds containing sulfur atoms only bound to two nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/636,371 US4479002A (en) | 1975-12-01 | 1975-12-01 | Carbamate-carbamoyl fluoride compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH619928A5 true CH619928A5 (xx) | 1980-10-31 |
Family
ID=24551598
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1505776A CH619928A5 (xx) | 1975-12-01 | 1976-11-30 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4479002A (xx) |
| JP (1) | JPS599548B2 (xx) |
| AT (1) | AT354461B (xx) |
| AU (1) | AU503185B2 (xx) |
| BE (1) | BE848910A (xx) |
| BR (1) | BR7607996A (xx) |
| CA (1) | CA1069128A (xx) |
| CH (1) | CH619928A5 (xx) |
| DE (1) | DE2654313A1 (xx) |
| DK (1) | DK537876A (xx) |
| ES (2) | ES453779A1 (xx) |
| FR (1) | FR2333790A1 (xx) |
| GB (1) | GB1506090A (xx) |
| IL (1) | IL51002A (xx) |
| IN (1) | IN145272B (xx) |
| IT (1) | IT1069142B (xx) |
| NL (1) | NL7613325A (xx) |
| SE (1) | SE7613427L (xx) |
| SU (1) | SU886737A3 (xx) |
| ZA (1) | ZA766573B (xx) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4234580A (en) * | 1977-03-28 | 1980-11-18 | Union Carbide Corporation | Carbamate thiosulfenylcarbamoyl fluoride compounds |
| US4268520A (en) | 1978-04-24 | 1981-05-19 | E. I. Du Pont De Nemours And Company | Insecticidal and nematicidal carbamates |
| US4127605A (en) * | 1978-04-24 | 1978-11-28 | E. I. Du Pont De Nemours And Company | Substituted carbamate intermediate |
| US4225615A (en) * | 1978-04-24 | 1980-09-30 | E. I. Du Pont De Nemours And Company | Insecticidal and nematicidal carbamates |
| DE3041725C2 (de) * | 1980-11-05 | 1984-11-29 | Standard Elektrik Lorenz Ag, 7000 Stuttgart | Gestell der Vertikalbauweise |
| JP4663233B2 (ja) * | 2001-11-09 | 2011-04-06 | エンゾン，インコーポレーテッド | ベンジル脱離系を利用する高分子チオール結合プロドラッグ |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3812174A (en) * | 1970-07-14 | 1974-05-21 | Chevron Res | Substituted aryl carbamates |
| DE2254359A1 (de) * | 1972-11-07 | 1974-05-16 | Bayer Ag | N-sulfenylierte carbamate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide |
| DE2530439C2 (de) * | 1974-07-11 | 1983-03-03 | CIBA-GEIGY AG, 4002 Basel | Bis-[0-(1-Alkylthio-äthylimino)-N-methyl-carbaminsäure]-N,N'-sulfide, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Schädlingsbekämpfungsmittel |
-
1975
- 1975-12-01 US US05/636,371 patent/US4479002A/en not_active Expired - Lifetime
-
1976
- 1976-11-02 ZA ZA766573A patent/ZA766573B/xx unknown
- 1976-11-04 CA CA265,087A patent/CA1069128A/en not_active Expired
- 1976-11-26 IL IL51002A patent/IL51002A/xx unknown
- 1976-11-29 AU AU20058/76A patent/AU503185B2/en not_active Expired
- 1976-11-30 SE SE7613427A patent/SE7613427L/xx not_active Application Discontinuation
- 1976-11-30 JP JP51143046A patent/JPS599548B2/ja not_active Expired
- 1976-11-30 IT IT69859/76A patent/IT1069142B/it active
- 1976-11-30 FR FR7636082A patent/FR2333790A1/fr active Granted
- 1976-11-30 DK DK537876A patent/DK537876A/da unknown
- 1976-11-30 AT AT885076A patent/AT354461B/de not_active IP Right Cessation
- 1976-11-30 CH CH1505776A patent/CH619928A5/fr not_active IP Right Cessation
- 1976-11-30 BR BR7607996A patent/BR7607996A/pt unknown
- 1976-11-30 SU SU762424152A patent/SU886737A3/ru active
- 1976-11-30 GB GB49811/76A patent/GB1506090A/en not_active Expired
- 1976-11-30 DE DE19762654313 patent/DE2654313A1/de not_active Withdrawn
- 1976-11-30 NL NL7613325A patent/NL7613325A/xx not_active Application Discontinuation
- 1976-11-30 BE BE172842A patent/BE848910A/xx not_active IP Right Cessation
- 1976-11-30 IN IN2135/CAL/1976A patent/IN145272B/en unknown
- 1976-11-30 ES ES453779A patent/ES453779A1/es not_active Expired
-
1977
- 1977-04-13 ES ES457744A patent/ES457744A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| FR2333790A1 (fr) | 1977-07-01 |
| IT1069142B (it) | 1985-03-25 |
| IL51002A0 (en) | 1977-01-31 |
| JPS5268126A (en) | 1977-06-06 |
| AT354461B (de) | 1979-01-10 |
| GB1506090A (en) | 1978-04-05 |
| ES457744A1 (es) | 1978-02-16 |
| ES453779A1 (es) | 1977-11-01 |
| IL51002A (en) | 1982-09-30 |
| US4479002A (en) | 1984-10-23 |
| ZA766573B (en) | 1977-10-26 |
| CA1069128A (en) | 1980-01-01 |
| JPS599548B2 (ja) | 1984-03-03 |
| DK537876A (da) | 1977-06-02 |
| NL7613325A (nl) | 1977-06-03 |
| AU2005876A (en) | 1978-06-08 |
| FR2333790B1 (xx) | 1981-01-09 |
| ATA885076A (de) | 1979-06-15 |
| AU503185B2 (en) | 1979-08-23 |
| DE2654313A1 (de) | 1977-06-08 |
| BR7607996A (pt) | 1977-11-08 |
| BE848910A (fr) | 1977-05-31 |
| SU886737A3 (ru) | 1981-11-30 |
| SE7613427L (sv) | 1977-06-02 |
| IN145272B (xx) | 1978-09-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0152360A2 (fr) | Nouveaux dérivés du cyano-2 benzimidazole, leur préparation et leur utilisation comme fongicides | |
| CH619689A5 (xx) | ||
| CH619928A5 (xx) | ||
| EP0119892B1 (fr) | Nouveau dérivés de l'hydroxylamine, leur procédé de préparation, leur application comme facteur de croissance des végétaux et les compositions les renfermant | |
| EP0265305B1 (fr) | Nouveaux dérivés de la 5-pyrazolone, leur procédé de préparation, leur utilisation comme herbicides et les compositions les renfermant | |
| FR2495609A1 (fr) | Acylurees, procedes pour les preparer et produits insecticides contenant de tels composes | |
| FR2559766A1 (fr) | Procede de preparation de derives de l'acide carbamique | |
| CH615417A5 (xx) | ||
| CH620425A5 (en) | Process for the preparation of new carbamatesulphenylcarbamoyl fluorides | |
| EP0155862B1 (fr) | Procédé de préparation de dérivés de l'acide carbamique | |
| EP0122206A2 (fr) | Nouveaux dérivés de cyano-2 imidazopyridine, leur préparation et leur utilisation comme fongicides | |
| CH369442A (fr) | Procédé de préparation de mono- et dicarbamates de 2,2-dichloro-1-aryl-1,3-prpane-diols | |
| EP0334720B1 (fr) | Nouveau procédé de préparation d'isocyanates d'acyle | |
| EP0585165B1 (fr) | Procédé de préparation d'isocyanates d'acyle | |
| CA1065892A (fr) | Urees herbicides, procede de preparation et compositions herbicides | |
| FR2635776A1 (fr) | Derives amides, procede pour leur fabrication et compositions fongicides les contenant | |
| BE799932A (fr) | Nouvelles 6-amino-s-triazinediones utiles comme herbicdes | |
| FR2560193A1 (fr) | Derives d'aminodiaryl sulfoxyde, procede pour leur preparation et compositions pharmaceutiques et pesticides les contenant | |
| CH621542A5 (en) | Process for the preparation of isothioureidobenzenes | |
| FR2483419A1 (fr) | Procede de preparation de la n-(2-(2-thenoyl)-thiopropionyl)-glicine | |
| CH653016A5 (fr) | Derives du chlorure d'aminosulfenyle, procede pour la preparation de ceux-ci et utilisation de ces derives pour la preparation de carbamates. | |
| EP0131522B1 (fr) | Nouveaux uraciles substitués comportant en position 1 un groupement phényloxy carbonyl substitué, leur préparation et les compositions herbicides les renfermant | |
| FR2494686A1 (fr) | Formamidocarbamates, procedes pour leur preparation et leur utilisation en tant que pesticides | |
| BE583616A (xx) | ||
| FR2660308A1 (fr) | Nouveaux derives soufres du 5,6-dihydro 2-methyl 4-[3-(trifluoromethyl) phenyl] 2h-1,2,4-oxadiazin-3(4h)-one, leur procede de preparation et les intermediaires de ce procede, leur application a titre d'herbicide et les compositions les renfermant. |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |