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943-59-9

943-59-9

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943-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943-59-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 943-59:
(5*9)+(4*4)+(3*3)+(2*5)+(1*9)=89
89 % 10 = 9
So 943-59-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClO2/c11-6-7-13-10(12)8-9-4-2-1-3-5-9/h1-5H,6-8H2

943-59-9SDS

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 2-chloroethyl 2-phenylacetate

1.2 Other means of identification

Product number -
Other names Benzeneacetic acid, 2-chloroethyl ester

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:943-59-9 SDS

943-59-9Relevant articles and documents

Method for generating ester through reaction of acyl chloride and 1,2-dichloroethane

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Paragraph 0023; 0025; 0059; 0060; 0061, (2017/08/30)

The invention discloses a method for generating ester through reaction of acyl chloride and 1,2-dichloroethane. The method comprises the following steps: taking acyl chloride, 1,2-dichloroethane and carbonate as reaction substrates, and taking 4-dimethyla

Zinc-Promoted Selective Cleavage of Ethers in Presence of Acyl Chloride

Bhar, Sanjay,Ranu, Brindaban C.

, p. 745 - 747 (2007/10/02)

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Reaction of 2-Alkyl-2-phenyl-1,3-dioxolans with Iodine Monochloride: Formation of α-Phenylalkanoate Esters

Goosen, Andre,McCleland, Cedric W.

, p. 1311 - 1312 (2007/10/02)

2-Alkyl-2-phenyl-1,3-dioxolans undergo a high-yield transformation into 2-chloroethyl α-phenylalkanoates upon treatment with iodine monochloride in dichloromethane.

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