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2-Oxetanone, 3-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27150-91-0

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27150-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27150-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,5 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 27150-91:
(7*2)+(6*7)+(5*1)+(4*5)+(3*0)+(2*9)+(1*1)=100
100 % 10 = 0
So 27150-91-0 is a valid CAS Registry Number.

27150-91-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyloxetan-2-one

1.2 Other means of identification

Product number -
Other names 2-Oxetanone,3-phenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:27150-91-0 SDS

27150-91-0Relevant academic research and scientific papers

1-Iodomethyl-3,4-diphenyl-2,6-dioxabicyclo[2.2.0]hexane: The first example of a [2.2.0] fused ketal

Wang, Gan,Wang, Ying,Arcari, Joel T.,Howell, Amy R.,Rheingold, Arnold L.,Concolino, Thomas

, p. 7051 - 7053 (1999)

The preparation of 1-iodomethyl-3,4-diphenyl-2,6- dioxabicyclo[2.2.0]hexane (12) is described. This represents the first reported example of a [2.2.0] fused ketal. The key step involved the iodoetherification of a 2-methyleneoxetane 11 containing a pendan

THE REACTION OF SMALL RING COMPOUND WITH CARBON MONOXIDE. THE CARBONYLATION OF OXIRANE

Kamiya, Yoshio,Kawato, Katsuhito,Ohta, Hiroyuki

, p. 1549 - 1552 (1980)

The carbonylation of oxiranes catalyzed by rhodium complex afforded β-lactones.Various factors which control the above reaction are presented.

HETEROCYCLYL-SUBSTITUTED OXETANES FOR THE TREATMENT OF PROLIFERATIVE OR INFECTIOUS DISEASES

-

Page/Page column 28, (2008/06/13)

Oxetane-containing nucleosides, particularly non-reducing psiconucleoside oxetanes (1) are described herein. Therapeutic application of these oxetane compounds toward the treatment of nucleoside analog related disorders such as disorders involving cellular proliferation and infection are also described.

Enzymatic kinetic resolution of tropic acid

Klomp, Dirk,Peters, Joop A.,Hanefeld, Ulf

, p. 3892 - 3896 (2007/10/03)

A new strategy has been developed for the CAL-B catalysed kinetic resolution of tropic acid by which both enantiomers of tropic acid can be obtained in good enantiomeric excess. (R)-Tropic acid was synthesised with 90% ee and (S)-tropic acid butyl ester in 99% ee by the hydrolysis of tropic acid butyl ester. The other enantiomers were available through the enzymatically catalysed reaction of tropic acid lactone with butanol to give (S)-tropic acid lactone and (R)-tropic acid ester in >98% ee.

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