SU247293A1 - - Google Patents
Info
- Publication number
- SU247293A1 SU247293A1 SU1217927A SU1217927A SU247293A1 SU 247293 A1 SU247293 A1 SU 247293A1 SU 1217927 A SU1217927 A SU 1217927A SU 1217927 A SU1217927 A SU 1217927A SU 247293 A1 SU247293 A1 SU 247293A1
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- aldrin
- aldrinic
- acetic acid
- literature
- Prior art date
Links
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- 239000002253 acid Substances 0.000 description 11
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 238000000034 method Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 3
- 239000012286 potassium permanganate Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- SIWNEELMSUHJGO-UHFFFAOYSA-N 2-(4-bromophenyl)-4,5,6,7-tetrahydro-[1,3]oxazolo[4,5-c]pyridine Chemical compound C1=CC(Br)=CC=C1C(O1)=NC2=C1CCNC2 SIWNEELMSUHJGO-UHFFFAOYSA-N 0.000 description 1
- JBIJLHTVPXGSAM-UHFFFAOYSA-N 2-naphthylamine Chemical compound C1=CC=CC2=CC(N)=CC=C21 JBIJLHTVPXGSAM-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000006149 azo coupling reaction Methods 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- -1 diazonium cation Chemical class 0.000 description 1
- 238000006193 diazotization reaction Methods 0.000 description 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 description 1
- 229950006824 dieldrin Drugs 0.000 description 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000012259 ether extract Substances 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 238000001727 in vivo Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 231100000663 medical toxicology Toxicity 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000012544 monitoring process Methods 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- CTRLRINCMYICJO-UHFFFAOYSA-N phenyl azide Chemical compound [N-]=[N+]=NC1=CC=CC=C1 CTRLRINCMYICJO-UHFFFAOYSA-N 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU247293A1 true SU247293A1 (https=) |
Family
ID=
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Corson et al. | Reactions of alpha, beta-unsaturated dinitriles | |
| DE1958123B2 (de) | Verfahren zur herstellung von 1-aminoalkan-1,1-diphosphonsaeuren oder deren salzen | |
| EP0055689B1 (de) | In 3-Stellung substituierte 2,4,6-trihalogenierte Benzamide und deren Salze, deren Herstellung und Verwendung als Ersatzstoffe für natürliche Süssstoffe sowie Süssungsmittel auf Basis dieser Verbindungen | |
| SU247293A1 (https=) | ||
| SU501667A3 (ru) | Способ получени монометиламинов | |
| Chiles et al. | Optically Active Diazo Compounds. Ii | |
| CH257403A (de) | Verfahren zur Herstellung von d,l-Methionin. | |
| EP0032540B1 (de) | 2-Methyl-3-(2,4,6-trijod-3-(1-morpholinoäthylidenamino)-benzamido)-propionitril, Verfahren zu dessen Herstellung und dessen Verwendung als Zwischenprodukt | |
| DE2516267C2 (de) | Verfahren zur Herstellung von 2-(4- Isobutylphenyl)-propiohydroxamsäure | |
| DE608434C (de) | Verfahren zur Darstellung von Kondensationsprodukten aus 2,3-Oxynaphthoesaeure und Anthranilsaeureamid bzw. seinen Substitutionsprodukten | |
| SU971090A3 (ru) | Способ получени производных пирогаллола | |
| SU436820A1 (ru) | Способ получени производных 3-формил-5-окси-(ацилокси)-индолов | |
| SU123531A1 (ru) | Способ получени 6-метоксиндола | |
| DE2329957A1 (de) | Verfahren zum reinigen von glyoxal | |
| SU289728A1 (ru) | Способ получения 1-амино-2,4-дихлорантрахинона | |
| SU435189A1 (ru) | СПОСОБ ПОЛУЧЕНИЯ ФОСФАТА ХРОМАВ П Т Б,i-.j^«| г» f.;';":;s7;"!'!TRnЧ-У-'Д и;;..;';11Г S УЗ | |
| AT94833B (de) | Verfahren zur Herstellung von Gerbmitteln. | |
| SU659082A3 (ru) | Способ получени диэтиламиноацетата п-ацетамидофенола или его хлоргидрата | |
| SU164288A1 (ru) | Способ получения ы- | |
| SU274108A1 (ru) | Способ получения з.з^-дикарбоксидифенил- 4,41-дитиогликолевой кислоты | |
| SU299507A1 (ru) | Способ получения 4,5,6,7-тетрафторгетероауксина | |
| SU245072A1 (ru) | Способ получения флуорантил-4-уксусной кислоты | |
| AT332982B (de) | Verfahren zur herstellung von neuen 17-hydroxy-7-(niederalkoxy)-carbonyl-3-oxo-17alfa-pregn-4-en-21-carbonsauren und deren salzen | |
| Brown | The Action of Salicylic Aldehyde on Sodium Pyrotartrate in Presence of Acetic Anhydride | |
| CH425787A (de) | Verfahren zur Herstellung von 3,4-Dihydroxymethyl-5-hydroxy-6-methylpyridin (Vitamin B6) |