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Merck
CN

152021

苯氧基-2-丙酮

97%

别名:

苯氧基丙酮

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关于此项目

线性分子式:
C6H5OCH2COCH3
化学文摘社编号:
分子量:
150.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-712-5
MDL number:
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产品名称

苯氧基-2-丙酮, 97%

InChI key

QWAVNXZAQASOML-UHFFFAOYSA-N

InChI

1S/C9H10O2/c1-8(10)7-11-9-5-3-2-4-6-9/h2-6H,7H2,1H3

SMILES string

CC(=O)COc1ccccc1

assay

97%

form

liquid

refractive index

n20/D 1.521 (lit.)

bp

229-230 °C (lit.)

density

1.097 g/mL at 25 °C (lit.)

Application

Phenoxy-2-propanone was used in the preparation of 3-mercapto-5-methyl-1-phenoxy-methyl-4-phenyl-1,2,4-triazolinium hydroxide inner salt.

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

185.0 °F - closed cup

flash_point_c

85 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propanones.
A Dafforn et al.
Biochemical and biophysical research communications, 104(2), 597-602 (1982-01-29)
Oxidative cyclisation of ketone thiosemicarbazones. II. Derivatives of phenoxyacetone.
J K Landquist
Journal of the Chemical Society. Perkin transactions 1, 2, 323-324 (1970-01-01)
Wesley Böhmer et al.
Advanced synthesis & catalysis, 362(9), 1858-1867 (2020-05-19)
Compared with biocatalysis in aqueous media, the use of enzymes in neat organic solvents enables increased solubility of hydrophobic substrates and can lead to more favorable thermodynamic equilibria, avoidance of possible hydrolytic side reactions and easier product recovery. ω-Transaminases from
Hong Ren et al.
Journal of biotechnology, 241, 33-41 (2016-11-14)
Asymmetric synthesis of chiral amines by amine dehydrogenases (AmDH), which catalyzed reductive amination of ketones with high enantioselectivity, is an ideal route for production of chiral amine. In this study, a facile approach is proposed to immobilize unstable amine dehydrogenase

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