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2-(4-氰基苯基)-2-氧代乙酸乙酯

2-(4-氰基苯基)-2-氧代乙酸乙酯名称

[ CAS 号 ]:
302912-31-8

[ 中文名 ]:
4-氰基苯甲酰甲酸乙酯

[ 英文名 ]:
Ethyl (4-cyanophenyl)(oxo)acetate

[中文别名 ]:

[英文别名 ]:

MFCD01319614
ethyl 2-(4-cyanophenyl)-2-oxo-acetate
Ethyl (4-cyanophenyl)(oxo)acetate
(4-cyano-phenyl)-oxo-acetic acid ethyl ester
Ethyl 2-(4-cyanophenyl)-2-oxoacetate
ethyl (4-cyanophenyl)glyoxylate
Ethyl 4-cyanobenzoylformate
Benzeneacetic acid, 4-cyano-α-oxo-, ethyl ester
ethyl (4-cyanophenyl)-oxo-acetate

2-(4-氰基苯基)-2-氧代乙酸乙酯物理化学性质

[ 密度 ]:
1.2±0.1 g/cm3

[ 沸点 ]:
350.3±25.0 °C at 760 mmHg

[ 分子式 ]:
C₁₁H₉NO₃

[ 分子量 ]:
203.194

[ 闪点 ]:
153.0±13.4 °C

[ 精确质量 ]:
203.058243

[ PSA ]:
67.16000

[ LogP ]:
1.45

[ 蒸汽压 ]:
0.0±0.8 mmHg at 25°C

[ 折射率 ]:
1.536

[ 储存条件 ]:
2-8°C

2-(4-氰基苯基)-2-氧代乙酸乙酯MSDS

2-(4-氰基苯基)-2-氧代乙酸乙酯安全信息

[ 个人防护装备 ]:
Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi

[ 危险品运输编码 ]:
NONH for all modes of transport

[ 海关编码 ]:
2926909090

2-(4-氰基苯基)-2-氧代乙酸乙酯合成路线

2-(4-氰基苯基)-2-氧代乙酸乙酯上下游产品

2-(4-氰基苯基)-2-氧代乙酸乙酯上游产品

2-(4-氰基苯基)-2-氧代乙酸乙酯下游产品

2-(4-氰基苯基)-2-氧代乙酸乙酯海关

[ 海关编码 ]: 2926909090

[ 中文概述 ]:
2926909090 其他腈基化合物. 增值税率:17.0% 退税率:9.0% 监管条件:无最惠国关税:6.5% 普通关税:30.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

2-(4-氰基苯基)-2-氧代乙酸乙酯文献

Harnessing Candida tenuis and Pichia stipitis in whole-cell bioreductions of o-chloroacetophenone: stereoselectivity, cell activity, in situ substrate supply and product removal.

Biotechnol. J. 8(6) , 699-708, (2013)

Generally, recombinant and native microorganisms can be employed as whole-cell catalysts. The application of native hosts, however, shortens the process development time by avoiding multiple steps of ...

Whole-cell bioreduction of aromatic alpha-keto esters using Candida tenuis xylose reductase and Candida boidinii formate dehydrogenase co-expressed in Escherichia coli.

Microb. Cell Fact. 7 , 37, (2008)

Whole cell-catalyzed biotransformation is a clear process option for the production of chiral alcohols via enantioselective reduction of precursor ketones. A wide variety of synthetically useful reduc...

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