152021
Phenoxy-2-propanone
97%
Sinónimos:
Phenoxyacetone
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About This Item
Fórmula lineal:
C6H5OCH2COCH3
Número de CAS:
Peso molecular:
150.17
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
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.)
SMILES string
CC(=O)COc1ccccc1
InChI
1S/C9H10O2/c1-8(10)7-11-9-5-3-2-4-6-9/h2-6H,7H2,1H3
InChI key
QWAVNXZAQASOML-UHFFFAOYSA-N
Categorías relacionadas
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.
Storage Class
10 - Combustible liquids
wgk_germany
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
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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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