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3-Thiophenecarboxylic acid, 2-methyl-5-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62664-44-2

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62664-44-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62664-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,6 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62664-44:
(7*6)+(6*2)+(5*6)+(4*6)+(3*4)+(2*4)+(1*4)=132
132 % 10 = 2
So 62664-44-2 is a valid CAS Registry Number.

62664-44-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-methyl-5-phenylthiophene-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Thiophenecarboxylic acid,2-methyl-5-phenyl-,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:62664-44-2 SDS

62664-44-2Downstream Products

62664-44-2Relevant academic research and scientific papers

One-Pot Synthesis of 2,3,5-Trisubstituted Thiophenes through Three-Component Assembly of Arylacetaldehydes, Elemental Sulfur, and 1,3-Dicarbonyls

Wang, Zilong,Qu, Zhonghua,Xiao, Fuhong,Huang, Huawen,Deng, Guo-Jun

supporting information, p. 796 - 800 (2018/02/21)

The three-component reaction for the synthesis of 2-arylthiophenes has been developed. Easily available arylacetaldehydes, 1,3-dicarbonyls, and elemental sulfur were directly assembled through cascade condensation/ annulation under base conditions. The pr

Copper-Catalyzed Coupling of 2-Siloxy-1-alkenes and Diazocarbonyl Compounds: Approach to Multisubstituted Furans, Pyrroles, and Thiophenes

Tan, Wei Wen,Yoshikai, Naohiko

, p. 5566 - 5573 (2016/07/14)

We report herein copper(II)-catalyzed cyclization reactions of silyl enol ethers derived from methyl ketones with α-diazo-β-ketoesters or α-diazoketones to afford 2-siloxy-2,3-dihydrofuran derivatives or 2,3,5-trisubstituted furans, respectively, under mild conditions. The former cyclization products serve as versatile 1,4-diketone surrogates, allowing facile preparation of 2,3,5-trisubstituted furans, pyrroles, and thiophenes.

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