(R)-1-(4-氯苯基)乙醇
(R)-1-(4-氯苯基)乙醇结构式
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常用名 | (R)-1-(4-氯苯基)乙醇 | 英文名 | 1-(4-Chlorophenyl)ethanol |
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| CAS号 | 75968-40-0 | 分子量 | 156.609 | |
| 密度 | 1.2±0.1 g/cm3 | 沸点 | 240.6±15.0 °C at 760 mmHg | |
| 分子式 | C8H9ClO | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | 99.3±20.4 °C | |
| 符号 |
GHS05, GHS07 |
信号词 | Danger |
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A novel carbonyl reductase with anti-Prelog stereospecificity from Acetobacter sp. CCTCC M209061: purification and characterization.
PLoS ONE 9(4) , e94543, (2014) A novel carbonyl reductase (AcCR) catalyzing the asymmetric reduction of ketones to enantiopure alcohols with anti-Prelog stereoselectivity was found in Acetobacter sp. CCTCC M209061 and enriched 27.5-fold with an overall yield of 0.4% by purification. The en... |
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Immobilization of Acetobacter sp. CCTCC M209061 for efficient asymmetric reduction of ketones and biocatalyst recycling.
Microb. Cell Fact. 11 , 119, (2012) The bacterium Acetobacter sp. CCTCC M209061 is a promising whole-cell biocatalyst with exclusive anti-Prelog stereoselectivity for the reduction of prochiral ketones that can be used to make valuable chiral alcohols such as (R)-4-(trimethylsilyl)-3-butyn-2-ol... |
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Optimization of culture conditions to produce high yields of active Acetobacter sp. CCTCC M209061 cells for anti-Prelog reduction of prochiral ketones.
BMC Biotechnol. 11 , 110, (2011) Chiral alcohols are widely used in the synthesis of chiral pharmaceuticals, flavors and functional materials and appropriate whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to these valuable compounds. The recently isolated ... |