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Метил 2-оксоциклогексанкарбоксила
- английское имяMethyl 2-oxocyclohexanecarboxylate
- CAS №41302-34-5
- CBNumberCB4458515
- ФормулаC8H12O3
- мольный вес156.18
- EINECS255-306-9
- номер MDLMFCD00077699
- файл Mol41302-34-5.mol
химическое свойство
Температура кипения | 50 °C/0.2 mmHg (lit.) |
плотность | 1.10 g/mL at 20 °C (lit.) |
показатель преломления | n |
Fp | 85 °C |
температура хранения | Inert atmosphere,Store in freezer, under -20°C |
форма | Liquid |
пка | 12.04±0.20(Predicted) |
цвет | Clear colorless to slightly yellow |
БРН | 510258 |
InChI | InChI=1S/C8H12O3/c1-11-8(10)6-4-2-3-5-7(6)9/h6H,2-5H2,1H3 |
ИнЧИКей | JEENWEAPRWGXSG-UHFFFAOYSA-N |
SMILES | C1(C(OC)=O)CCCCC1=O |
LogP | 0.290 (est) |
Система регистрации веществ EPA | Cyclohexanecarboxylic acid, 2-oxo-, methyl ester (41302-34-5) |
UNSPSC Code | 12352100 |
NACRES | NA.22 |
Заявления о безопасности | 23-24/25 |
РИДАДР | NA 1993 / PGIII |
WGK Германия | 3 |
кода HS | 29183000 |
Метил 2-оксоциклогексанкарбоксила химические свойства, назначение, производство
Химические свойства
clear colorless to slightly yellow liquidИспользование
Methyl 2-Oxocyclohexanecarboxylate is a novel intermediate for the preparation of TRPA1 antagonists for treatment of pain and other TRPA1-associated diseases.Ссылки на синтез
Journal of the American Chemical Society, 102, p. 431, 1980 DOI: 10.1021/ja00521a100Organic Syntheses, Coll. Vol. 7, p. 351, 1990
Синтез
The flask is flushed with nitrogen and charged with 18.02 g (0.20 mol) of dimethyl carbonate, 50 mL of anhydrous tetrahydrofuran, and 6.12 g (0.25 mol) of sodium hydride. The suspension is stirred and heated to reflux temperature, at which time the slow, dropwise addition of 7.80 g (0.080 mol) of cyclohexanone in 20 mL of dry tetrahydrofuran is begun. After 2 min, 0.306 g (0.0076 mol) of powdered potassium hydride is added to initiate the reaction. The addition of cyclohexanone is continued over a 1-hr period. The mixture is stirred and heated at reflux for another 30 min, cooled in an ice bath for 15–20 min, and hydrolyzed by slowly adding 75 mL of 3 M aqueous acetic acid. The flask's contents are poured into 100 mL of aqueous sodium chloride, and the aqueous mixture is extracted with four 150-mL portions of chloroform. The organic layers are combined, dried with anhydrous sodium sulfate, and concentrated at room temperature with a rotary evaporator. Distillation of the residual liquid under reduced pressure gives 9.8–10.8 g (79–87%) of methyl 2-oxocyclohexanecarboxylate as a colorless liquid, bp 53–55°C.Метил 2-оксоциклогексанкарбоксила запасные части и сырье
Метил 2-оксоциклогексанкарбоксила поставщик
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