方案
99%
SMILES字符串
OC(C(O)=O)c1ccccc1
InChI
1S/C8H8O3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7,9H,(H,10,11)
InChI key
IWYDHOAUDWTVEP-UHFFFAOYSA-N
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警示用语：
Danger
危险声明
危险分类
Eye Dam. 1
储存分类代码
13 - Non Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
此项目有
[Mandelic acid in urine].
H Igisu et al.
Nihon rinsho. Japanese journal of clinical medicine, 57 Suppl, 454-456 (1999-09-30)
[Mandelic acid in urine].
Hideki Igisu et al.
Nihon rinsho. Japanese journal of clinical medicine, 62 Suppl 12, 482-484 (2005-01-22)
Huihui Sun et al.
Biotechnology letters, 37(8), 1655-1661 (2015-04-10)
To examine nitrilase-mediated hydrolysis of nitriles to produce optically pure α-hydroxycarboxylic acids. A novel nitrilase, GPnor51, from Luminiphilus syltensis NOR5-1B was discovered by genomic data mining. It could hydrolyze racemic o-chloromandelonitrile to (R)-o-chloromandelic acid with high enantioselectivity (ee 98.2 %).
Hualei Wang et al.
Applied and environmental microbiology, 81(24), 8469-8477 (2015-10-04)
The nitrilase-mediated pathway has significant advantages in the production of optically pure aromatic α-hydroxy carboxylic acids. However, low enantioselectivity and activity are observed on hydrolyzing o-chloromandelonitrile to produce optically pure (R)-o-chloromandelic acid. In the present study, a protein engineering approach
Dima Albals et al.
Electrophoresis, 35(19), 2807-2818 (2014-07-02)
A generic chiral separation strategy for the analysis of acidic compounds in CEC is proposed in completion of an earlier defined strategy for nonacidic compounds. The screening step of this strategy uses a 45 mM ammonium formate (pH 2.9)/ACN (35/65
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