FI78460C - Cykloalkanderivat, foerfarande foer deras framstaellning och kompositioner innehaollande dessa. - Google Patents
Cykloalkanderivat, foerfarande foer deras framstaellning och kompositioner innehaollande dessa. Download PDFInfo
- Publication number
- FI78460C FI78460C FI831428A FI831428A FI78460C FI 78460 C FI78460 C FI 78460C FI 831428 A FI831428 A FI 831428A FI 831428 A FI831428 A FI 831428A FI 78460 C FI78460 C FI 78460C
- Authority
- FI
- Finland
- Prior art keywords
- general formula
- group
- hydrazine
- derivatives
- alkoxy
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 35
- 238000002360 preparation method Methods 0.000 title claims description 19
- 238000000034 method Methods 0.000 title claims description 12
- 150000001924 cycloalkanes Chemical class 0.000 title claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 50
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 20
- -1 p-methoxyphenylmethylidene Chemical group 0.000 claims description 19
- 239000004480 active ingredient Substances 0.000 claims description 17
- 241001465754 Metazoa Species 0.000 claims description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 230000004584 weight gain Effects 0.000 claims description 10
- 235000019786 weight gain Nutrition 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 150000002576 ketones Chemical class 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 150000002429 hydrazines Chemical class 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 4
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- 125000003277 amino group Chemical group 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 29
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
- 239000011541 reaction mixture Substances 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- 239000013078 crystal Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
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- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 description 4
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
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- 239000008240 homogeneous mixture Substances 0.000 description 4
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- 239000007858 starting material Substances 0.000 description 4
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- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 3
- BCZXFFBUYPCTSJ-UHFFFAOYSA-L Calcium propionate Chemical compound [Ca+2].CCC([O-])=O.CCC([O-])=O BCZXFFBUYPCTSJ-UHFFFAOYSA-L 0.000 description 3
- 229920002261 Corn starch Polymers 0.000 description 3
- 235000019739 Dicalciumphosphate Nutrition 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229920002472 Starch Polymers 0.000 description 3
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 3
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- 239000002585 base Substances 0.000 description 3
- 229910000019 calcium carbonate Inorganic materials 0.000 description 3
- FUFJGUQYACFECW-UHFFFAOYSA-L calcium hydrogenphosphate Chemical compound [Ca+2].OP([O-])([O-])=O FUFJGUQYACFECW-UHFFFAOYSA-L 0.000 description 3
- 239000004330 calcium propionate Substances 0.000 description 3
- 235000010331 calcium propionate Nutrition 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229910000390 dicalcium phosphate Inorganic materials 0.000 description 3
- 229940038472 dicalcium phosphate Drugs 0.000 description 3
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 3
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
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- 150000007530 organic bases Chemical class 0.000 description 3
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- 239000000377 silicon dioxide Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
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- 239000000080 wetting agent Substances 0.000 description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 2
- VCDPHYIZVFJQCD-UHFFFAOYSA-N 2-benzylidenecyclohexan-1-one Chemical compound O=C1CCCCC1=CC1=CC=CC=C1 VCDPHYIZVFJQCD-UHFFFAOYSA-N 0.000 description 2
- 239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 description 2
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- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
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- XHEXTNNXHJUONB-UHFFFAOYSA-N 2-[(3,4-dimethoxyphenyl)methylidene]cyclohexan-1-one Chemical compound C1=C(OC)C(OC)=CC=C1C=C1C(=O)CCCC1 XHEXTNNXHJUONB-UHFFFAOYSA-N 0.000 description 1
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- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- FNIATMYXUPOJRW-UHFFFAOYSA-N cyclohexylidene Chemical group [C]1CCCCC1 FNIATMYXUPOJRW-UHFFFAOYSA-N 0.000 description 1
- PWAPCRSSMCLZHG-UHFFFAOYSA-N cyclopentylidene Chemical group [C]1CCCC1 PWAPCRSSMCLZHG-UHFFFAOYSA-N 0.000 description 1
- UVDOIWXDCYNLJD-UHFFFAOYSA-N cyclopentylidenemethylbenzene Chemical compound C1CCCC1=CC1=CC=CC=C1 UVDOIWXDCYNLJD-UHFFFAOYSA-N 0.000 description 1
- 125000004177 diethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- IDAGXRIGDWCIET-SDFKWCIISA-L disodium;(2s,3s,4s,5r)-2,3,4,5-tetrahydroxyhexanedioate Chemical compound [Na+].[Na+].[O-]C(=O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C([O-])=O IDAGXRIGDWCIET-SDFKWCIISA-L 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- LIAWOTKNAVAKCX-UHFFFAOYSA-N hydrazine;dihydrochloride Chemical compound Cl.Cl.NN LIAWOTKNAVAKCX-UHFFFAOYSA-N 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000013372 meat Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- YASIJFAGZYQWTN-UHFFFAOYSA-N methyl n-[(2-benzylcyclohexylidene)amino]carbamate Chemical compound COC(=O)NN=C1CCCCC1CC1=CC=CC=C1 YASIJFAGZYQWTN-UHFFFAOYSA-N 0.000 description 1
- ZJWCWQGIDALZTE-UHFFFAOYSA-N methyl n-[(2-benzylidenecycloheptylidene)amino]carbamate Chemical compound COC(=O)NN=C1CCCCCC1=CC1=CC=CC=C1 ZJWCWQGIDALZTE-UHFFFAOYSA-N 0.000 description 1
- ZISUGUOYUUAVNS-UHFFFAOYSA-N methyl n-[[2-[(4-chlorophenyl)methylidene]cyclohexylidene]amino]carbamate Chemical compound COC(=O)NN=C1CCCCC1=CC1=CC=C(Cl)C=C1 ZISUGUOYUUAVNS-UHFFFAOYSA-N 0.000 description 1
- HERIZXMFTXDDRV-UHFFFAOYSA-N methyl n-[[2-[(4-methoxyphenyl)methylidene]cyclohexylidene]amino]carbamate Chemical compound COC(=O)NN=C1CCCCC1=CC1=CC=C(OC)C=C1 HERIZXMFTXDDRV-UHFFFAOYSA-N 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910000150 monocalcium phosphate Inorganic materials 0.000 description 1
- 235000019691 monocalcium phosphate Nutrition 0.000 description 1
- IRJPRWAEHYOHMU-UHFFFAOYSA-N n-[(2-benzylidenecyclohexylidene)amino]-4-hexoxy-3,5-dimethoxybenzamide Chemical compound C1=C(OC)C(OCCCCCC)=C(OC)C=C1C(=O)NN=C(CCCC1)C1=CC1=CC=CC=C1 IRJPRWAEHYOHMU-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 125000001639 phenylmethylene group Chemical group [H]C(=*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 244000144977 poultry Species 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 239000002516 radical scavenger Substances 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
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 229940032147 starch Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- 229960000984 tocofersolan Drugs 0.000 description 1
- AOBORMOPSGHCAX-DGHZZKTQSA-N tocofersolan Chemical compound OCCOC(=O)CCC(=O)OC1=C(C)C(C)=C2O[C@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C AOBORMOPSGHCAX-DGHZZKTQSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000012711 vitamin K3 Nutrition 0.000 description 1
- 239000011652 vitamin K3 Substances 0.000 description 1
- 235000015099 wheat brans Nutrition 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/72—Hydrazones
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/105—Aliphatic or alicyclic compounds
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/30—Feeding-stuffs specially adapted for particular animals for swines
Landscapes
- Chemical & Material Sciences (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Husbandry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Food Science & Technology (AREA)
- Birds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fodder In General (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU138082 | 1982-05-04 | ||
| HU821380A HU190384B (en) | 1982-05-04 | 1982-05-04 | Process for preparing cycloalkane derivatives and compositions for weight increasing containing such compounds |
Publications (4)
| Publication Number | Publication Date |
|---|---|
| FI831428A0 FI831428A0 (fi) | 1983-04-26 |
| FI831428L FI831428L (fi) | 1983-11-05 |
| FI78460B FI78460B (fi) | 1989-04-28 |
| FI78460C true FI78460C (fi) | 1989-08-10 |
Family
ID=10954197
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI831428A FI78460C (fi) | 1982-05-04 | 1983-04-26 | Cykloalkanderivat, foerfarande foer deras framstaellning och kompositioner innehaollande dessa. |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US4587261A (en, 2012) |
| JP (1) | JPS5936649A (en, 2012) |
| AU (1) | AU558694B2 (en, 2012) |
| BE (1) | BE896628A (en, 2012) |
| CA (1) | CA1244045A (en, 2012) |
| CH (1) | CH659245A5 (en, 2012) |
| CS (1) | CS239937B2 (en, 2012) |
| DD (1) | DD209813A5 (en, 2012) |
| DE (1) | DE3316317A1 (en, 2012) |
| DK (1) | DK197083A (en, 2012) |
| ES (1) | ES8506595A1 (en, 2012) |
| FI (1) | FI78460C (en, 2012) |
| FR (1) | FR2526425B1 (en, 2012) |
| GB (1) | GB2119798B (en, 2012) |
| GR (1) | GR79216B (en, 2012) |
| HU (1) | HU190384B (en, 2012) |
| IT (1) | IT1194224B (en, 2012) |
| NL (1) | NL8301546A (en, 2012) |
| PH (1) | PH19132A (en, 2012) |
| PL (1) | PL138303B1 (en, 2012) |
| SE (1) | SE462283B (en, 2012) |
| SU (1) | SU1274620A3 (en, 2012) |
| YU (1) | YU42856B (en, 2012) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU190795B (en) * | 1982-05-04 | 1986-11-28 | Egyt Gyogyszervegyeszeti Gyar,Hu | Process for producing carbazinic derivatives and compositions containing them for increasing weight yield |
| HU192633B (en) * | 1984-12-12 | 1987-06-29 | Egyt Gyogyszervegyeszeti Gyar | Process for producing carbazinic acid derivatives and compositions containing them for increasing weight-yield |
| FR2649101B1 (fr) * | 1989-06-30 | 1994-10-28 | Rhone Poulenc Agrochimie | Azolylmethylcyclohexane benzilidene et utilisation comme fongicide |
| CA2006309C (fr) * | 1988-12-29 | 2001-12-18 | Jean Hutt | Azolylmethylcyclopentane benzylidene fongicide |
| ES2103166B1 (es) * | 1992-08-26 | 1998-04-01 | Ciba Geigy Ag | Procedimiento para la obtencion de amidinohidrazonas biciclicas. |
| US7809076B1 (en) * | 2005-03-11 | 2010-10-05 | Adtran, Inc. | Adaptive interference canceling system and method |
| CN107960532A (zh) * | 2016-10-20 | 2018-04-27 | 湖南晶天科技实业有限公司 | 一种饲料添加剂与一种饲料 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1085028A (fr) * | 1952-10-08 | 1955-01-26 | Lepetit Spa | Procédé pour la préparation de cycloalcoylidène-hydrazides des acides monocarboxyliques |
| DE2122572A1 (de) * | 1971-05-07 | 1972-11-23 | Farbenfabriken Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von neuen Derivaten von 2-Formyl-3-carbonatnido-chinoxalin-di-N-oxiden sowie ihre Verwendung als Arzneimittel und Futtermittelzusatz |
| HU171738B (hu) * | 1975-03-14 | 1978-03-28 | Egyt Gyogyszervegyeszeti Gyar | Sposob poluchenija proizvodnykh kinoksalin-1,4-dioksid-azometina |
| GB1504151A (en) * | 1975-04-17 | 1978-03-15 | Ici Ltd | Methods using and compositions containing quinone derivatives for use in animal husbandry |
| US4041070A (en) * | 1976-07-14 | 1977-08-09 | American Cyanamid Company | Tetrahydro-4-imino-1-naphthylureas |
| US4236017A (en) * | 1979-07-27 | 1980-11-25 | Montedison S.P.A., | Process for synthesizing 2-substituted semicarbazones and carbalkoxy hydrazones |
-
1982
- 1982-05-04 HU HU821380A patent/HU190384B/hu not_active IP Right Cessation
-
1983
- 1983-04-20 CS CS832828A patent/CS239937B2/cs unknown
- 1983-04-22 PH PH28806A patent/PH19132A/en unknown
- 1983-04-26 FI FI831428A patent/FI78460C/fi not_active IP Right Cessation
- 1983-04-28 YU YU966/83A patent/YU42856B/xx unknown
- 1983-05-02 CH CH2348/83A patent/CH659245A5/de not_active IP Right Cessation
- 1983-05-02 SE SE8302480A patent/SE462283B/sv not_active IP Right Cessation
- 1983-05-02 BE BE1/10779A patent/BE896628A/fr not_active IP Right Cessation
- 1983-05-03 NL NL8301546A patent/NL8301546A/nl not_active Application Discontinuation
- 1983-05-03 DK DK197083A patent/DK197083A/da not_active Application Discontinuation
- 1983-05-03 PL PL1983241759A patent/PL138303B1/pl unknown
- 1983-05-03 GB GB08312049A patent/GB2119798B/en not_active Expired
- 1983-05-03 ES ES522057A patent/ES8506595A1/es not_active Expired
- 1983-05-03 AU AU14191/83A patent/AU558694B2/en not_active Ceased
- 1983-05-03 GR GR71276A patent/GR79216B/el unknown
- 1983-05-03 CA CA000427275A patent/CA1244045A/en not_active Expired
- 1983-05-03 IT IT20920/83A patent/IT1194224B/it active
- 1983-05-03 FR FR8307326A patent/FR2526425B1/fr not_active Expired
- 1983-05-03 US US06/491,083 patent/US4587261A/en not_active Expired - Fee Related
- 1983-05-04 DE DE19833316317 patent/DE3316317A1/de active Granted
- 1983-05-04 SU SU833590059A patent/SU1274620A3/ru active
- 1983-05-04 JP JP58077652A patent/JPS5936649A/ja active Pending
- 1983-05-04 DD DD83250606A patent/DD209813A5/de not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: E GY T GYOGYSZERVEGYESZETI GYAR |