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63762-45-8

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63762-45-8 Usage

Chemical compound

2,5-Thiophenedicarboxylic acid, 3-methyl-, dimethyl ester

Primary use

Reagent or intermediate in organic synthesis

Synthesis

Reaction of 2,5-thiophenedicarboxylic acid and methanol in the presence of a catalyst

Physical appearance

Colorless to pale yellow liquid

Odor

Strong

Commercial use

Not widely used in commercial products

Applications

Research and development in pharmaceuticals, agrochemicals, and other industries

Potential properties

Biological and pharmacological properties for further study and exploration

Check Digit Verification of cas no

The CAS Registry Mumber 63762-45-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,6 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63762-45:
(7*6)+(6*3)+(5*7)+(4*6)+(3*2)+(2*4)+(1*5)=138
138 % 10 = 8
So 63762-45-8 is a valid CAS Registry Number.

63762-45-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethyl 3-methyl-2,5-thiophenedicarboxylate

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:63762-45-8 SDS

63762-45-8Downstream Products

63762-45-8Relevant articles and documents

Synthesis of 2-thiophenecarboxylic and 2,5-thiophenedicarboxylic acid esters via the reaction of thiophenes with the CCl4-ROH reagent in the presence of vanadium, iron, and molybdenum catalysts

Khusnutdinov,Shchadneva,Baiguzina,Mukminov,Mayakova,Smirnov,Dzhemilev

experimental part, p. 471 - 478 (2010/03/31)

2-Thiophenecarboxylic and 2,5-thiohenedicarboxylic acid esters were synthesized via the reaction of thiophene with the CCl4-ROH-catalyst system, with a total yield of 44-85%. A possible reaction scheme includes the successive steps of alkylation of thiophene with carbon tetrachloride, leading to 2-trichloromethylthiophene, and alcoholysis of the product giving the corresponding 2-thiophenecarboxylate. The best catalysts for this reaction are VO(acac)2, Fe(acac)3, and Mo(CO)6.

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