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
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
EC Number:
241-240-8
Beilstein/REAXYS Number:
2208678
MDL number:
Assay:
≥99%
Form:
crystals
Quality Level
product line
ReagentPlus®
assay
≥99%
form
crystals
mp
131-134 °C (lit.), 132-138 °C
functional group
carboxylic acid, hydroxyl, phenyl
SMILES string
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
Application
(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.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>374.0 °F
flash_point_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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 778052-25G | 04061832940687 |
| 778052-100G | 04061832940670 |