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2-chloroethyl 2-chlorobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

58133-38-3

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58133-38-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58133-38-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,1,3 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 58133-38:
(7*5)+(6*8)+(5*1)+(4*3)+(3*3)+(2*3)+(1*8)=123
123 % 10 = 3
So 58133-38-3 is a valid CAS Registry Number.

58133-38-3SDS

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-chlorobenzoate

1.2 Other means of identification

Product number -
Other names 2-chloro-benzoic acid-(2-chloro-ethyl 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:58133-38-3 SDS

58133-38-3Downstream Products

58133-38-3Relevant academic research and scientific papers

A Three-Phase Four-Component Coupling Reaction: Selective Synthesis of o-Chloro Benzoates by KCl, Arynes, CO2, and Chloroalkanes

Jiang, Huanfeng,Zhang, Yu,Xiong, Wenfang,Cen, Jinghe,Wang, Lu,Cheng, Ruixiang,Qi, Chaorong,Wu, Wanqing

supporting information, p. 345 - 349 (2019/01/24)

A transition-metal-free three-phase four-component coupling reaction (3P-4CR) involving KCl, arynes, chloroalkanes and CO2 has been reported for the first time, enabling the incorporation of both chloro and CO2 into an aryne simultaneously. The reactions for the synthesis of different types of o-chloro benzoates can be selectively modulated by the chloroalkane utilized. The corresponding products can be alternatively transformed for postsynthetic functionalizations conveniently.

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

-

Paragraph 0023; 0025; 0044; 0045; 0046, (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.

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