SU561492A3 - Добавка к корму или питьевой воде дл домашней птицы - Google Patents

Добавка к корму или питьевой воде дл домашней птицы

Info

Publication number: SU561492A3
Authority: SU; USSR - Soviet Union
Prior art keywords: hydrogen; acid; ester; hydroxy; feed
Prior art date: 1968-06-14

Application number

SU1488051A

Other languages

English (en)

Russian (ru)

Inventor

Херберт Мицони Ренат

Де Стивенс Джорж

Original Assignee

Циба-Гейги Аг (Фирма)

Priority date (The priority date 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 date listed.)

1968-06-14

Filing date

1970-10-22

Publication date

1977-06-05

1970-10-22 Application filed by Циба-Гейги Аг (Фирма) filed Critical Циба-Гейги Аг (Фирма)

1977-06-05 Application granted granted Critical

1977-06-05 Publication of SU561492A3 publication Critical patent/SU561492A3/ru

Links

239000000654 additive Substances 0.000 title claims description 12
230000000996 additive effect Effects 0.000 title claims description 9
239000003651 drinking water Substances 0.000 title claims description 6
235000020188 drinking water Nutrition 0.000 title claims description 6
244000144977 poultry Species 0.000 title claims description 4
-1 trifluoromethyl mercapto group Chemical group 0.000 claims description 46
125000000217 alkyl group Chemical group 0.000 claims description 43
229910052739 hydrogen Inorganic materials 0.000 claims description 32
239000001257 hydrogen Substances 0.000 claims description 32
239000002253 acid Substances 0.000 claims description 25
150000001875 compounds Chemical class 0.000 claims description 22
150000002148 esters Chemical class 0.000 claims description 22
125000004432 carbon atom Chemical group C* 0.000 claims description 19
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 17
125000001931 aliphatic group Chemical group 0.000 claims description 16
125000003118 aryl group Chemical group 0.000 claims description 11
125000003342 alkenyl group Chemical group 0.000 claims description 8
125000003545 alkoxy group Chemical group 0.000 claims description 8
125000000753 cycloalkyl group Chemical group 0.000 claims description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
125000005843 halogen group Chemical group 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
150000004820 halides Chemical class 0.000 claims description 6
229910052760 oxygen Inorganic materials 0.000 claims description 6
239000001301 oxygen Substances 0.000 claims description 6
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
125000002947 alkylene group Chemical group 0.000 claims description 5
125000003710 aryl alkyl group Chemical group 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
229910052736 halogen Inorganic materials 0.000 claims description 5
150000002367 halogens Chemical class 0.000 claims description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
125000004663 dialkyl amino group Chemical group 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
239000011593 sulfur Substances 0.000 claims description 4
125000002030 1,2-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([*:2])C([H])=C1[H] 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
125000000392 cycloalkenyl group Chemical group 0.000 claims description 3
125000005842 heteroatom Chemical group 0.000 claims description 3
125000004433 nitrogen atom Chemical group N* 0.000 claims description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
125000004438 haloalkoxy group Chemical group 0.000 claims description 2
229910052751 metal Inorganic materials 0.000 claims description 2
239000002184 metal Substances 0.000 claims description 2
150000003839 salts Chemical class 0.000 claims 19
239000000203 mixture Substances 0.000 claims 16
150000002431 hydrogen Chemical class 0.000 claims 15
231100000252 nontoxic Toxicity 0.000 claims 14
230000003000 nontoxic effect Effects 0.000 claims 14
125000004494 ethyl ester group Chemical group 0.000 claims 9
229910052784 alkaline earth metal Inorganic materials 0.000 claims 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
239000013543 active substance Substances 0.000 claims 6
125000005907 alkyl ester group Chemical group 0.000 claims 5
150000007513 acids Chemical class 0.000 claims 4
239000003513 alkali Substances 0.000 claims 4
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims 3
244000068988 Glycine max Species 0.000 claims 3
235000010469 Glycine max Nutrition 0.000 claims 3
235000013305 food Nutrition 0.000 claims 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims 2
240000008042 Zea mays Species 0.000 claims 2
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 claims 2
235000002017 Zea mays subsp mays Nutrition 0.000 claims 2
150000001342 alkaline earth metals Chemical class 0.000 claims 2
150000001408 amides Chemical class 0.000 claims 2
150000003863 ammonium salts Chemical class 0.000 claims 2
229910052791 calcium Inorganic materials 0.000 claims 2
239000011575 calcium Substances 0.000 claims 2
125000001589 carboacyl group Chemical group 0.000 claims 2
235000005822 corn Nutrition 0.000 claims 2
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 2
235000013312 flour Nutrition 0.000 claims 2
150000002430 hydrocarbons Chemical group 0.000 claims 2
150000004702 methyl esters Chemical class 0.000 claims 2
150000002825 nitriles Chemical class 0.000 claims 2
229910052757 nitrogen Inorganic materials 0.000 claims 2
125000005447 octyloxy group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])O* 0.000 claims 2
125000005429 oxyalkyl group Chemical group 0.000 claims 2
102000004169 proteins and genes Human genes 0.000 claims 2
108090000623 proteins and genes Proteins 0.000 claims 2
239000002904 solvent Substances 0.000 claims 2
229940088594 vitamin Drugs 0.000 claims 2
239000011782 vitamin Substances 0.000 claims 2
238000005406 washing Methods 0.000 claims 2
AGWCYWWMYBRXRH-UHFFFAOYSA-N 2-dodecoxy-4-oxo-1H-quinoline-3-carboxylic acid Chemical compound CCCCCCCCCCCCOC1=C(C(=O)C2=CC=CC=C2N1)C(=O)O AGWCYWWMYBRXRH-UHFFFAOYSA-N 0.000 claims 1
XOQQVKDBGLYPGH-UHFFFAOYSA-N 2-oxo-1h-quinoline-3-carboxylic acid Chemical compound C1=CC=C2NC(=O)C(C(=O)O)=CC2=C1 XOQQVKDBGLYPGH-UHFFFAOYSA-N 0.000 claims 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims 1
239000004215 Carbon black (E152) Substances 0.000 claims 1
ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 claims 1
OIFBSDVPJOWBCH-UHFFFAOYSA-N Diethyl carbonate Chemical compound CCOC(=O)OCC OIFBSDVPJOWBCH-UHFFFAOYSA-N 0.000 claims 1
235000019733 Fish meal Nutrition 0.000 claims 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims 1
240000004658 Medicago sativa Species 0.000 claims 1
235000017587 Medicago sativa ssp. sativa Nutrition 0.000 claims 1
241001465754 Metazoa Species 0.000 claims 1
241000521582 Paralvinella palmiformis Species 0.000 claims 1
206010033799 Paralysis Diseases 0.000 claims 1
AUNGANRZJHBGPY-SCRDCRAPSA-N Riboflavin Chemical compound OC[C@@H](O)[C@@H](O)[C@@H](O)CN1C=2C=C(C)C(C)=CC=2N=C2C1=NC(=O)NC2=O AUNGANRZJHBGPY-SCRDCRAPSA-N 0.000 claims 1
239000005862 Whey Substances 0.000 claims 1
102000007544 Whey Proteins Human genes 0.000 claims 1
108010046377 Whey Proteins Proteins 0.000 claims 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims 1
229910052783 alkali metal Inorganic materials 0.000 claims 1
150000001340 alkali metals Chemical class 0.000 claims 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims 1
239000003674 animal food additive Substances 0.000 claims 1
125000004429 atom Chemical group 0.000 claims 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
125000004122 cyclic group Chemical group 0.000 claims 1
ZAKOWWREFLAJOT-UHFFFAOYSA-N d-alpha-Tocopheryl acetate Natural products CC(=O)OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-UHFFFAOYSA-N 0.000 claims 1
125000006612 decyloxy group Chemical group 0.000 claims 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
DLLJVQNYBYOKGS-UHFFFAOYSA-N ethoxyethane;pentane Chemical compound CCCCC.CCOCC DLLJVQNYBYOKGS-UHFFFAOYSA-N 0.000 claims 1
238000000605 extraction Methods 0.000 claims 1
239000004467 fishmeal Substances 0.000 claims 1
238000005188 flotation Methods 0.000 claims 1
230000002641 glycemic effect Effects 0.000 claims 1
239000007970 homogeneous dispersion Substances 0.000 claims 1
229940042795 hydrazides for tuberculosis treatment Drugs 0.000 claims 1
229930195733 hydrocarbon Natural products 0.000 claims 1
229910052748 manganese Inorganic materials 0.000 claims 1
239000011572 manganese Substances 0.000 claims 1
239000000463 material Substances 0.000 claims 1
239000000155 melt Substances 0.000 claims 1
229930182817 methionine Natural products 0.000 claims 1
150000004682 monohydrates Chemical class 0.000 claims 1
239000011734 sodium Substances 0.000 claims 1
239000011780 sodium chloride Substances 0.000 claims 1
235000012424 soybean oil Nutrition 0.000 claims 1
239000003549 soybean oil Substances 0.000 claims 1
238000003756 stirring Methods 0.000 claims 1
FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 claims 1
229940124530 sulfonamide Drugs 0.000 claims 1
239000013589 supplement Substances 0.000 claims 1
229940042585 tocopherol acetate Drugs 0.000 claims 1
229930003231 vitamin Natural products 0.000 claims 1
235000013343 vitamin Nutrition 0.000 claims 1
150000003722 vitamin derivatives Chemical class 0.000 claims 1
239000011701 zinc Substances 0.000 claims 1
229910052725 zinc Inorganic materials 0.000 claims 1
125000001183 hydrocarbyl group Chemical group 0.000 description 10
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
229910052731 fluorine Inorganic materials 0.000 description 4
239000011737 fluorine Substances 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
125000003396 thiol group Chemical group [H]S* 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 2
125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000005976 1-phenylethyloxy group Chemical group 0.000 description 1
125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
125000005975 2-phenylethyloxy group Chemical group 0.000 description 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
125000003302 alkenyloxy group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
125000005336 allyloxy group Chemical group 0.000 description 1
125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
125000002993 cycloalkylene group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
125000004030 farnesyl group Chemical group [H]C([*])([H])C([H])=C(C([H])([H])[H])C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000002350 geranyl group Chemical group [H]C([*])([H])/C([H])=C(C([H])([H])[H])/C([H])([H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000002510 isobutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])O* 0.000 description 1
125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 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
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
125000003884 phenylalkyl group Chemical group 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000005505 thiomorpholino group Chemical group 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/233—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 4
- 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
- A23K20/116—Heterocyclic compounds
- A23K20/132—Heterocyclic compounds containing only one nitrogen as hetero atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/44—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by —CHO groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
- C07C43/205—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring the aromatic ring being a non-condensed ring
- C07C43/2055—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring the aromatic ring being a non-condensed ring containing more than one ether bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/008—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with tri- or tetrahalomethyl compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
- C07D215/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Polymers & Plastics (AREA)
Life Sciences & Earth Sciences (AREA)
Engineering & Computer Science (AREA)
Food Science & Technology (AREA)
Chemical Kinetics & Catalysis (AREA)
Animal Husbandry (AREA)
Zoology (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Fodder In General (AREA)
Feed For Specific Animals (AREA)
Quinoline Compounds (AREA)
Physical Water Treatments (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Plural Heterocyclic Compounds (AREA)

SU1488051A 1968-06-14 1970-10-22 Добавка к корму или питьевой воде дл домашней птицы SU561492A3 (ru)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date
US73696268A	1968-06-14	1968-06-14
US77042668A	1968-10-24	1968-10-24
US80833369A	1969-03-18	1969-03-18

Publications (1)

Publication Number	Publication Date
SU561492A3 true SU561492A3 (ru)	1977-06-05

Family

ID=27419219

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SU1488051A SU561492A3 (ru)	1968-06-14	1970-10-22	Добавка к корму или питьевой воде дл домашней птицы

Country Status (18)

Country	Link
JP (1)	JPS504673B1 (cs)
AT (2)	AT301547B (cs)
BE (1)	BE734566A (cs)
CH (2)	CH560193A5 (cs)
DE (1)	DE1929165A1 (cs)
ES (1)	ES368288A2 (cs)
FI (1)	FI49407C (cs)
FR (1)	FR2010879B1 (cs)
GB (2)	GB1270413A (cs)
IE (1)	IE33810B1 (cs)
IL (1)	IL32362A0 (cs)
KE (2)	KE2547A (cs)
MY (2)	MY7500153A (cs)
NL (1)	NL6908370A (cs)
NO (2)	NO132868C (cs)
RO (1)	RO56838A (cs)
SE (2)	SE362424B (cs)
SU (1)	SU561492A3 (cs)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1980001068A1 (fr) *	1978-11-27	1980-05-29	Orch Sinteza I	3-(2,2,2-trimethylhydrazine) propionate, sa methode de production et son utilisation

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS58219166A (ja) *	1982-06-14	1983-12-20	Nippon Shinyaku Co Ltd	４−キノロン誘導体
EP0262305B1 (en) *	1986-08-29	1990-10-31	American Cyanamid Company	Method for the preparation of anilinofumarate and quinoline-2,3-dicarboxylic acid
RU2341513C2 (ru)	2001-06-12	2008-12-20	Веллстат Терапьютикс Корпорейшн	Соединения для лечения метаболических заболеваний
MX2016012467A (es) *	2014-03-26	2016-12-20	Procter & Gamble	Sistemas de perfume.

1969
- 1969-05-12 CH CH724969A patent/CH560193A5/xx not_active IP Right Cessation
- 1969-06-02 NL NL6908370A patent/NL6908370A/xx not_active Application Discontinuation
- 1969-06-08 IL IL32362A patent/IL32362A0/xx unknown
- 1969-06-09 DE DE19691929165 patent/DE1929165A1/de active Pending
- 1969-06-10 FR FR6919073A patent/FR2010879B1/fr not_active Expired
- 1969-06-11 SE SE08293/69A patent/SE362424B/xx unknown
- 1969-06-11 IE IE800/69A patent/IE33810B1/xx unknown
- 1969-06-11 SE SE7206919A patent/SE387223B/xx unknown
- 1969-06-12 ES ES368288A patent/ES368288A2/es not_active Expired
- 1969-06-13 AT AT563069A patent/AT301547B/de not_active IP Right Cessation
- 1969-06-13 JP JP44046446A patent/JPS504673B1/ja active Pending
- 1969-06-13 NO NO2456/69A patent/NO132868C/no unknown
- 1969-06-13 FI FI691755A patent/FI49407C/fi active
- 1969-06-13 BE BE734566D patent/BE734566A/xx unknown
- 1969-06-13 AT AT01300/71A patent/AT319725B/de not_active IP Right Cessation
- 1969-06-14 RO RO60235A patent/RO56838A/ro unknown
- 1969-06-16 GB GB9653/70A patent/GB1270413A/en not_active Expired
- 1969-06-16 GB GB30403/69A patent/GB1270412A/en not_active Expired
1970
- 1970-10-22 SU SU1488051A patent/SU561492A3/ru active
1973
- 1973-03-16 NO NO1068/73A patent/NO137072C/no unknown
1974
- 1974-06-20 CH CH846174A patent/CH610732A5/xx not_active IP Right Cessation
1975
- 1975-07-16 KE KE2547*UA patent/KE2547A/xx unknown
- 1975-07-16 KE KE2548*UA patent/KE2548A/xx unknown
- 1975-12-30 MY MY153/75A patent/MY7500153A/xx unknown
- 1975-12-30 MY MY154/75A patent/MY7500154A/xx unknown

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
WO1980001068A1 (fr) *	1978-11-27	1980-05-29	Orch Sinteza I	3-(2,2,2-trimethylhydrazine) propionate, sa methode de production et son utilisation

Also Published As

Publication number	Publication date
KE2547A (en)	1975-08-01
FI49407C (fi)	1975-06-10
GB1270412A (en)	1972-04-12
CH610732A5 (en)	1979-05-15
MY7500154A (en)	1975-12-31
MY7500153A (en)	1975-12-31
GB1270413A (en)	1972-04-12
NO132868C (cs)	1976-01-21
FR2010879A1 (cs)	1970-02-20
BE734566A (cs)	1969-12-15
SE362424B (cs)	1973-12-10
SE387223B (sv)	1976-09-06
AT301547B (de)	1972-09-11
FI49407B (cs)	1975-02-28
RO56838A (cs)	1975-03-15
NO137072C (no)	1977-12-28
JPS504673B1 (cs)	1975-02-22
IE33810B1 (en)	1974-11-13
NL6908370A (cs)	1969-12-16
NO137072B (no)	1977-09-19
NO132868B (cs)	1975-10-13
AT319725B (de)	1975-01-10
KE2548A (en)	1975-08-01
IE33810L (en)	1969-12-14
IL32362A0 (en)	1969-08-27
FR2010879B1 (cs)	1976-09-03
DE1929165A1 (de)	1969-12-18
ES368288A2 (es)	1971-05-01
CH560193A5 (cs)	1975-03-27

Publication	Publication Date	Title
US3463858A (en)	1969-08-26	Organic zinc feed additive and method of making same
IL45123A (en)	1977-12-30	5-methyl-isoflavone-derivatives process for preparation thereof and pharmaceutical compositions containing them
DE1692414B2 (de)	1978-01-12	Gefluegelfuttermittel
WO1983000988A1 (fr)	1983-03-31	Additif d'alimentation ou produit d'alimentation
Grau et al.	1944	Requirement of Tryptophane by the Chick: One Figure
US3373038A (en)	1968-03-12	Estrogenic compounds and animal growth promoters
JPS5529958A (en)	1980-03-03	Feed for lobster
SU1635955A1 (ru)	1991-03-23	Способ приготовлени корма дл сельскохоз йственной птицы
JPS63169941A (ja)	1988-07-13	食肉用家禽の飼育方法
DE3020470A1 (de)	1980-12-04	Allyl- und propylderivate von recorcinylsaeurelakton-verbindungen und verfahren zu ihrer herstellung
US3021216A (en)	1962-02-13	Animal feed compositions
IL23314A (en)	1969-04-30	Esters of the antibiotic pleuro-mutilin,their production and animal feed supplement containing same
US4071534A (en)	1978-01-31	Process for producing l-ascorbic acid-2-sulfate
US4282228A (en)	1981-08-04	Animal feed and process
US3778508A (en)	1973-12-11	Feed compositions and methods
JP3148318B2 (ja)	2001-03-19	反すう動物の飼育方法
US3008873A (en)	1961-11-14	Controlled particle size of 4, 4-dinitrocarbanilide
US3025216A (en)	1962-03-13	Bacitracin compositions and production thereof
SU1709909A3 (ru)	1992-01-30	Способ получени производных /2-тиенилметил/-тиомочевины
US2929713A (en)	1960-03-22	Preparation of coumestrol esters and use thereof
US3803315A (en)	1974-04-09	Animal feed and process
US3915966A (en)	1975-10-28	Morpholino zearalins
SU745480A1 (ru)	1980-07-07	Способ получени кормовой добавки
DE2501875A1 (de)	1975-07-24	Alkylsulfonylmethyl- und alkylsulfinylmethylchinoxalin-1,4-dioxide
US2941884A (en)	1960-06-21	Animal feeds, animal feed supplements, and methods

SU561492A3 - Добавка к корму или питьевой воде дл домашней птицы - Google Patents

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Applications Claiming Priority (3)

Publications (1)

Family

ID=27419219

Family Applications (1)

Country Status (18)

Cited By (1)

Families Citing this family (4)

Cited By (1)

Also Published As

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