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197149

2-苯氧基丙酸

≥98%

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线性分子式:
C6H5OCH(CH3)CO2H
化学文摘社编号:
940-31-8
分子量:
166.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24851337
EC Number:
213-370-5
Beilstein/REAXYS Number:
5734971
MDL number:
MFCD00002643
Assay:
≥98%
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Quality Level

100

assay

≥98%

bp

265 °C (lit.)

mp

112-115 °C (lit.)

functional group

carboxylic acid, phenoxy

SMILES string

CC(Oc1ccccc1)C(O)=O

InChI

1S/C9H10O3/c1-7(9(10)11)12-8-5-3-2-4-6-8/h2-7H,1H3,(H,10,11)

InChI key

SXERGJJQSKIUIC-UHFFFAOYSA-N

General description

Solvent-induced invesrsion of enantioselectivity during esterification of 2-phenoxypropionic acid catalyzed by Candida cylindracea lipase has been investigated. Derivatives of 2-phenoxypropionic acid are potential herbicides.

存储类别

11 - Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
10107CR
14601EN
02607CO
02513CR
01727AN

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Manuel A P Segurado et al.
The Journal of organic chemistry, 72(14), 5327-5336 (2007-06-15)
Rate constants were measured for the oxidative chlorodehydrogenation of (R,S)-2-phenoxypropanoic acid and nine ortho-, ten para- and five meta-substituted derivatives using (R,S)-1-chloro-3-methyl-2,6-diphenylpiperidin-4-one (NCP) as chlorinating agent. The kinetics was run in 50% (v/v) aqueous acetic acid acidified with perchloric acid
Lipase-catalyzed production of optically active acids via asymmetric hydrolysis of esters.
Cambou B and Klibanov AM.
Applied Biochemistry and Biotechnology, 9(3), 255-260 (1984)
Solvent-induced inversion of enantiosflectivity in lipase-catalyzed esterification of 2-phenoxypropionic acids.
Ueji S, et al.
Biotechnology Letters, 14(3), 163-168 (1992)
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全球贸易项目编号

货号GTIN
197149-50G04061838762368