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2-Chloroethyl 2-phenylacetate is an organic compound with the chemical formula C10H11ClO2. It is a colorless liquid with a molecular weight of 200.65 g/mol. 2-chloroethyl 2-phenylacetate is formed by the esterification of 2-chloroethanol and 2-phenylacetic acid, resulting in an ester linkage between the two functional groups. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides and pesticides. Due to its reactivity, it is important to handle 2-chloroethyl 2-phenylacetate with care, as it may pose health risks and environmental concerns.

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 academic research and scientific papers

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

-

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

An Effective Method for the Construction of Esters Using Cs2CO3 as Oxygen Source

Ren, Lanhui,Wang, Lianyue,Lv, Ying,Li, Guosong,Gao, Shuang

supporting information, p. 5172 - 5175 (2015/11/24)

An effective method for the construction of esters from acyl chloride and halohydrocarbon using Cs2CO3 as an oxygen source was achieved for the first time. The methodology has a wide scope of substrates and can be scaled up. The study of a preliminary reaction mechanism demonstrated that the O in the products comes from Cs2CO3 and this esterification proceeds through a free radical reaction. It was also found that CO2 can also be used in this esterification reaction as an oxygen source.

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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