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152021

Sigma-Aldrich

Phenoxy-2-propanone

97%

Synonym(s):

Phenoxyacetone

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About This Item

Linear Formula:
C6H5OCH2COCH3
CAS Number:
621-87-4
Molecular Weight:
150.17
EC Number:
210-712-5
MDL number:
MFCD00008767
UNSPSC Code:
12352100
PubChem Substance ID:
24849191
NACRES:
NA.22

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

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 Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

185.0 °F - closed cup

Flash Point(C)

85 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ2121
STBJ1468
STBB0282V
STBB0282
S31446

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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
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)
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
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)

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