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Benzeneethanol, a-chloro-, acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

39773-55-2

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39773-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 39773-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,7,7 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 39773-55:
(7*3)+(6*9)+(5*7)+(4*7)+(3*3)+(2*5)+(1*5)=162
162 % 10 = 2
So 39773-55-2 is a valid CAS Registry Number.

39773-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1-chloroethyl acetate

1.2 Other means of identification

Product number -
Other names 1-chloro-2-penylethylacetate

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:39773-55-2 SDS

39773-55-2Relevant academic research and scientific papers

REACTIVE INTERMEDIATES IN THE PHOTOLYSIS AND THERMOLYSIS OF 3-CHLORO-3-BENZYLDIAZIRINE

Liu, Michael T. H.,Chishti, Najmul H.,Tencer, Michael,Tomioka, Hideo,Izawa, Yasuji

, p. 887 - 892 (2007/10/02)

The photochemical and thermal decomposition of 3-chloro-3-benzyldiazirine have been studied in different reaction conditions.The decomposition gives rise to benzylchlorocarbene which can rearrange to E and Z chlorostyrene and/or react with the environment.In the presence of acetic acid the main product is 1-chloro-2-phenylethyl acetate.Experiments with acetic acid-d4 showed that some of the chlorostyrene is formed from the carbocation; other experiments conducted with tetramethylethylene as a carbene trapping agent show that the carbene is formed even in the presence of acetic acid.

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