156728
6-甲氧基-4-二氢色原酮
97%
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关于此项目
经验公式（希尔记法）:
C10H10O2
化学文摘社编号:
分子量:
162.19
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
方案
97%
表单
solid
沸点
141-143 °C/13.5 mmHg (lit.)
mp
31-35 °C (lit.)
密度
1.071 g/mL at 25 °C (lit.)
官能团
ketone
SMILES字符串
Cc1ccc2OCCC(=O)c2c1
InChI
1S/C10H10O2/c1-7-2-3-10-8(6-7)9(11)4-5-12-10/h2-3,6H,4-5H2,1H3
InChI key
RJHXEPLSJAVTFW-UHFFFAOYSA-N
应用
The product has been used as a substrate for carbonyl reductase from Sporobolomyces salmonicolor, wherein it was reduced to the corresponding (R)-chiral alcohol. It has also been used as a substrate for the enantioselective reduction by 3 biocatalysts, namely, Didymosphaeria igniaria, Coryneum betulinum and Chaetomium sp.
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
法规信息
新产品
此项目有
Enantioselective reduction of 4-chromanone and its derivatives by selected filamentous fungi.
Janeczko T, et al.
Journal of Molecular Catalysis. B, Enzymatic, 97, 278-282 (2013)
Dunming Zhu et al.
Organic & biomolecular chemistry, 4(14), 2690-2695 (2006-07-11)
In our effort to search for effective carbonyl reductases, the activity and enantioselectivity of a carbonyl reductase from Sporobolomyces salmonicolor have been evaluated toward the reduction of a variety of ketones. This carbonyl reductase (SSCR) reduces a broad spectrum of
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