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2-Chloroethyl 3-methylbenzoate is an organic compound with the chemical formula C10H11ClO2. It is a colorless to pale yellow liquid with a molecular weight of 200.65 g/mol. 2-chloroethyl 3-methylbenzoate is characterized by the presence of a chloroethyl group (C2H4Cl) attached to a methylbenzoate moiety, which consists of a benzoic acid (C7H6O2) with a methyl group (CH3) attached to the third carbon. 2-Chloroethyl 3-methylbenzoate is synthesized through the esterification of 3-methylbenzoic acid with 2-chloroethanol and is used as an intermediate in the production of pharmaceuticals and agrochemicals. It is also known for its potential applications in the synthesis of various chemical compounds due to its unique structure.

6639-18-5

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6639-18-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6639-18-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,6,3 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6639-18:
(6*6)+(5*6)+(4*3)+(3*9)+(2*1)+(1*8)=115
115 % 10 = 5
So 6639-18-5 is a valid CAS Registry Number.

6639-18-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloroethyl 3-methylbenzoate

1.2 Other means of identification

Product number -
Other names -

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:6639-18-5 SDS

6639-18-5Downstream Products

6639-18-5Relevant academic research and scientific papers

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

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Paragraph 0023; 0025; 0026; 0027; 0028, (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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