778052
(S)-(+)-扁桃酸
ReagentPlus®, ≥99%
别名:
(S)-α-羟基苯乙酸
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关于此项目
线性分子式:
C6H5CH(OH)CO2H
CAS Number:
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
质量水平
产品线
ReagentPlus®
方案
≥99%
表单
crystals
mp
131-134 °C (lit.)
132-138 °C
官能团
carboxylic acid
hydroxyl
phenyl
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
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
>374.0 °F
闪点(°C)
> 190 °C
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
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)
Synthetic Communications, 23, 2761-2761 (1993)
The Journal of Organic Chemistry, 58, 2313-2313 (1993)
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