152021
Phenoxy-2-propanone
97%
Sinonimo/i:
Phenoxyacetone
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About This Item
Prodotti consigliati
Saggio
97%
Forma fisica
liquid
Indice di rifrazione
n20/D 1.521 (lit.)
P. eboll.
229-230 °C (lit.)
Densità
1.097 g/mL at 25 °C (lit.)
Stringa SMILE
CC(=O)COc1ccccc1
InChI
1S/C9H10O2/c1-8(10)7-11-9-5-3-2-4-6-9/h2-6H,7H2,1H3
QWAVNXZAQASOML-UHFFFAOYSA-N
Categorie correlate
Applicazioni
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.
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
185.0 °F - closed cup
Punto d’infiammabilità (°C)
85 °C - closed cup
Dispositivi di protezione individuale
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.
Biochemical and biophysical research communications, 104(2), 597-602 (1982-01-29)
Oxidative cyclisation of ketone thiosemicarbazones. II. Derivatives of phenoxyacetone.
Journal of the Chemical Society. Perkin transactions 1, 2, 323-324 (1970-01-01)
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
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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