所有图片(2)
别名:
(S)-α-羟基苯乙酸
线性分子式:
C6H5CH(OH)CO2H
CAS号:
分子量:
152.15
Beilstein:
2208678
EC 号:
MDL编号:
UNSPSC代码:
12352002
PubChem化学物质编号:
NACRES:
NA.22
推荐产品
质量水平
产品线
ReagentPlus®
检测方案
≥99%
形式
crystals
mp
131-134 °C (lit.)
132-138 °C
SMILES字符串
O[C@H](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)/t7-/m0/s1
InChI key
IWYDHOAUDWTVEP-ZETCQYMHSA-N
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应用
(S)-(+)-Mandelic acid can be used as a starting material to synthesize (S)-cyclohexenyl phenyl glycoxilic acid, an optically active tertiary α-hydroxy acid component of (S)-oxybutynin.
It is a versatile reagent used in the resolution of racemates and the preparation of amides.
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
警示用语：
Danger
危险声明
危险分类
Eye Dam. 1
WGK
WGK 3
闪点(°F)
>374.0 °F
闪点(°C)
> 190 °C
Tetrahedron, 50, 5049-5049 (1994)
Chiral mandelic acid template provides a highly practical solution for (S)-oxybutynin synthesis.
Grover P T, et al.
The Journal of Organic Chemistry, 65(19), 6283-6287 (2000)
Mara Reifenrath et al.
Metabolic engineering communications, 7, e00079-e00079 (2018-10-30)
Mandelic acid is an important aromatic fine chemical and is currently mainly produced via chemical synthesis. Recently, mandelic acid production was achieved by microbial fermentations using engineered Escherichia coli and Saccharomyces cerevisiae expressing heterologous hydroxymandelate synthases (hmaS). The best-performing strains
Synthetic Communications, 23, 2761-2761 (1993)
The Journal of Organic Chemistry, 58, 2313-2313 (1993)
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