DE2145317A1 - Zubereitungen auf basis stabilisierter phosphorsaeureester - Google Patents
Zubereitungen auf basis stabilisierter phosphorsaeureesterInfo
- Publication number
- DE2145317A1 DE2145317A1 DE2145317A DE2145317A DE2145317A1 DE 2145317 A1 DE2145317 A1 DE 2145317A1 DE 2145317 A DE2145317 A DE 2145317A DE 2145317 A DE2145317 A DE 2145317A DE 2145317 A1 DE2145317 A1 DE 2145317A1
- Authority
- DE
- Germany
- Prior art keywords
- group
- phosphoric acid
- preparation according
- acid ester
- carbon atoms
- 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.)
- Pending
Links
- 238000002360 preparation method Methods 0.000 title claims description 54
- 150000003014 phosphoric acid esters Chemical class 0.000 title claims description 53
- -1 alkyl radical Chemical class 0.000 claims description 71
- 125000004432 carbon atom Chemical group C* 0.000 claims description 49
- 239000011111 cardboard Substances 0.000 claims description 41
- 239000003381 stabilizer Substances 0.000 claims description 40
- 125000000217 alkyl group Chemical group 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 35
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical compound C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 claims description 32
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 30
- 229910052717 sulfur Inorganic materials 0.000 claims description 25
- 239000011593 sulfur Substances 0.000 claims description 24
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 23
- 239000002904 solvent Substances 0.000 claims description 22
- 150000002148 esters Chemical class 0.000 claims description 21
- 239000000203 mixture Substances 0.000 claims description 18
- 239000007787 solid Substances 0.000 claims description 16
- 239000001257 hydrogen Substances 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 230000000361 pesticidal effect Effects 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- 125000001931 aliphatic group Chemical group 0.000 claims description 10
- 239000000654 additive Substances 0.000 claims description 9
- 150000003464 sulfur compounds Chemical class 0.000 claims description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 8
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 8
- 125000004429 atom Chemical group 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 8
- 239000011707 mineral Substances 0.000 claims description 8
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 8
- 239000012188 paraffin wax Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 230000000087 stabilizing effect Effects 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
- 238000000354 decomposition reaction Methods 0.000 claims description 7
- 239000007788 liquid Substances 0.000 claims description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
- 230000000996 additive effect Effects 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 5
- 125000003342 alkenyl group Chemical group 0.000 claims description 5
- 239000000575 pesticide Substances 0.000 claims description 5
- XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 claims description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 5
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 claims description 4
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
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- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
- 238000009833 condensation Methods 0.000 claims description 4
- 230000005494 condensation Effects 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- UCQFCFPECQILOL-UHFFFAOYSA-N diethyl hydrogen phosphate Chemical compound CCOP(O)(=O)OCC UCQFCFPECQILOL-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 239000006259 organic additive Substances 0.000 claims description 4
- 235000019271 petrolatum Nutrition 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- 229920000573 polyethylene Polymers 0.000 claims description 4
- 229920005862 polyol Polymers 0.000 claims description 4
- 150000003077 polyols Chemical class 0.000 claims description 4
- 230000005588 protonation Effects 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 4
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
- 239000004593 Epoxy Substances 0.000 claims description 3
- 239000004264 Petrolatum Substances 0.000 claims description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 3
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- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
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- 150000002989 phenols Chemical class 0.000 claims description 3
- 239000008107 starch Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- BVZSTBILYMMKCG-UHFFFAOYSA-N 2,2-dichloroethenyl diethyl phosphate Chemical compound CCOP(=O)(OCC)OC=C(Cl)Cl BVZSTBILYMMKCG-UHFFFAOYSA-N 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 2
- 239000005995 Aluminium silicate Substances 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 2
- 229920001800 Shellac Polymers 0.000 claims description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims description 2
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 2
- 235000012211 aluminium silicate Nutrition 0.000 claims description 2
- 239000011449 brick Substances 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- 238000006243 chemical reaction Methods 0.000 claims description 2
- 239000010459 dolomite Substances 0.000 claims description 2
- 229910000514 dolomite Inorganic materials 0.000 claims description 2
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims description 2
- 239000000835 fiber Substances 0.000 claims description 2
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- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
- 239000004615 ingredient Substances 0.000 claims description 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 claims description 2
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- 150000008442 polyphenolic compounds Chemical class 0.000 claims description 2
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- 239000004814 polyurethane Substances 0.000 claims description 2
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- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 claims description 2
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- 125000001424 substituent group Chemical group 0.000 claims description 2
- 235000000346 sugar Nutrition 0.000 claims description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 2
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- 235000012239 silicon dioxide Nutrition 0.000 claims 2
- LKFSFDQXHZCZJE-UHFFFAOYSA-N (2-bromo-2-chloroethenyl) diethyl phosphate Chemical compound CCOP(=O)(OCC)OC=C(Cl)Br LKFSFDQXHZCZJE-UHFFFAOYSA-N 0.000 claims 1
- FTNJQNQLEGKTGD-ZFJHNFROSA-N 1,3-benzodioxole Chemical group C1O[13C]=2[13CH]=[13CH][13CH]=[13CH][13C]=2O1 FTNJQNQLEGKTGD-ZFJHNFROSA-N 0.000 claims 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 claims 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims 1
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 claims 1
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- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- 125000003375 sulfoxide group Chemical group 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000002025 wood fiber Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- XKMZOFXGLBYJLS-UHFFFAOYSA-L zinc;prop-2-enoate Chemical compound [Zn+2].[O-]C(=O)C=C.[O-]C(=O)C=C XKMZOFXGLBYJLS-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/091—Esters of phosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/025—Purification; Separation; Stabilisation; Desodorisation of organo-phosphorus compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/113—Esters of phosphoric acids with unsaturated acyclic alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7033013A FR2112069B1 (US07923587-20110412-C00001.png) | 1970-09-11 | 1970-09-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2145317A1 true DE2145317A1 (de) | 1973-02-08 |
Family
ID=9061188
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE2145317A Pending DE2145317A1 (de) | 1970-09-11 | 1971-09-10 | Zubereitungen auf basis stabilisierter phosphorsaeureester |
Country Status (17)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0281098A1 (en) * | 1987-03-04 | 1988-09-07 | Eisai Co., Ltd. | Benzodioxole derivatives, compositions comprising the same, and the use of the same for the manufacture of medicaments |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU71378A1 (US07923587-20110412-C00001.png) * | 1974-11-27 | 1976-09-06 | ||
| LU73337A1 (US07923587-20110412-C00001.png) * | 1975-09-05 | 1977-05-11 | ||
| DE2734108A1 (de) * | 1977-07-28 | 1979-02-08 | Bayer Ag | Insektizide und akarizide mittel |
| US5292901A (en) * | 1987-03-04 | 1994-03-08 | Eisai Co., Ltd. | Benzodioxole derivatives |
| JP5066915B2 (ja) * | 2006-04-03 | 2012-11-07 | 住友化学株式会社 | １，３−ベンズジオキソール化合物とその用途 |
| CN109400573B (zh) * | 2017-08-17 | 2023-04-11 | 中国人民解放军第二军医大学 | 苯并[d][1,3]二氧杂环戊烯类化合物、制备方法及其应用 |
| CN113045863A (zh) * | 2021-04-22 | 2021-06-29 | 襄阳银鼎电力设备有限责任公司 | 一种大直径芯棒及其制备方法 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2493927A (en) * | 1946-02-08 | 1950-01-10 | Thompson Boyce Plant Res | Methylenedioxyphenyl compound as insecticide, insect repellent, and pyrethrin synergist |
| US3116201A (en) * | 1952-02-29 | 1963-12-31 | Shell Oil Co | Organo-phosphorus insecticide |
| US2891889A (en) * | 1953-11-20 | 1959-06-23 | Union Carbide Corp | Insecticidal compositions containing cyclethrin |
| US2826530A (en) * | 1954-06-14 | 1958-03-11 | Gaines W Eddy | Synergistic insecticidal compositions comprising an 0, 0-di-alkyl thiophosphate-4-methylumbelliferone |
| US2904463A (en) * | 1958-01-20 | 1959-09-15 | Union Carbide Corp | Insecticidal compositions containing 1-naphthyl-n-methylcarbamate and sulfoxide as a synergist therefor |
| US3053729A (en) * | 1959-10-26 | 1962-09-11 | Shell Oil Co | Insecticidal compositions |
| NL131123C (US07923587-20110412-C00001.png) * | 1961-01-06 | |||
| NL276695A (US07923587-20110412-C00001.png) * | 1961-04-05 |
-
1970
- 1970-09-11 FR FR7033013A patent/FR2112069B1/fr not_active Expired
-
1971
- 1971-09-06 IL IL37667A patent/IL37667A/xx unknown
- 1971-09-08 AU AU33254/71A patent/AU468830B2/en not_active Expired
- 1971-09-08 ZA ZA715998A patent/ZA715998B/xx unknown
- 1971-09-09 LU LU63885A patent/LU63885A1/xx unknown
- 1971-09-10 ES ES394952A patent/ES394952A1/es not_active Expired
- 1971-09-10 GB GB1413274A patent/GB1369998A/en not_active Expired
- 1971-09-10 DE DE2145317A patent/DE2145317A1/de active Pending
- 1971-09-10 BE BE772456A patent/BE772456A/xx unknown
- 1971-09-10 AT AT789671A patent/AT313634B/de not_active IP Right Cessation
- 1971-09-10 CA CA122,522A patent/CA984288A/en not_active Expired
- 1971-09-10 GB GB4239971A patent/GB1369997A/en not_active Expired
- 1971-09-10 NL NL7112508A patent/NL7112508A/xx unknown
- 1971-09-10 IT IT52804/71A patent/IT942168B/it active
- 1971-09-10 BR BR5977/71A patent/BR7105977D0/pt unknown
- 1971-09-10 CH CH1331771A patent/CH573707A5/xx not_active IP Right Cessation
- 1971-09-10 OA OA54360A patent/OA03856A/xx unknown
- 1971-09-14 US US00180507A patent/US3852439A/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0281098A1 (en) * | 1987-03-04 | 1988-09-07 | Eisai Co., Ltd. | Benzodioxole derivatives, compositions comprising the same, and the use of the same for the manufacture of medicaments |
Also Published As
| Publication number | Publication date |
|---|---|
| ES394952A1 (es) | 1975-09-16 |
| NL7112508A (US07923587-20110412-C00001.png) | 1972-03-14 |
| GB1369997A (en) | 1974-10-09 |
| FR2112069A1 (US07923587-20110412-C00001.png) | 1972-06-16 |
| US3852439A (en) | 1974-12-03 |
| IL37667A (en) | 1975-06-25 |
| IT942168B (it) | 1973-03-20 |
| OA03856A (fr) | 1971-12-24 |
| CA984288A (en) | 1976-02-24 |
| BE772456A (fr) | 1972-03-10 |
| ZA715998B (en) | 1972-05-31 |
| AT313634B (de) | 1974-02-25 |
| AU468830B2 (en) | 1976-01-22 |
| LU63885A1 (US07923587-20110412-C00001.png) | 1973-03-09 |
| GB1369998A (en) | 1974-10-09 |
| AU3325471A (en) | 1973-03-15 |
| BR7105977D0 (pt) | 1973-04-05 |
| FR2112069B1 (US07923587-20110412-C00001.png) | 1973-12-21 |
| IL37667A0 (en) | 1971-11-29 |
| CH573707A5 (US07923587-20110412-C00001.png) | 1976-03-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| OHN | Withdrawal |