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3-Furancarboxylic acid, 4-methyl-2,5-diphenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62664-63-5

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62664-63-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62664-63-5 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, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 62664-63:
(7*6)+(6*2)+(5*6)+(4*6)+(3*4)+(2*6)+(1*3)=135
135 % 10 = 5
So 62664-63-5 is a valid CAS Registry Number.

62664-63-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 4-methyl-2,5-diphenylfuran-3-carboxylate

1.2 Other means of identification

Product number -
Other names 3-Furancarboxylic acid,4-methyl-2,5-diphenyl-,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:62664-63-5 SDS

62664-63-5Relevant academic research and scientific papers

Ionic liquid as catalyst and reaction medium: A Simple and Efficient Procedure for Paal-Knorr furan synthesis

Wang, Gangqiang,Guan, Zhi,Tang, Rongchang,He, Yanhong

, p. 370 - 377 (2010)

The ionic liquid 1-butyl-3-methyl-imidazolium hydrogen sulfate, [bmim]HSO4, efficiently catalyzes Paal-Knorr furan synthesis without any organic solvent. A wide range of aliphatic and aromatic 1,4-diketones easily undergo condensations to form furan derivatives, providing a general and convenient procedure. The Paal-Knorr reaction of ester-substituted 1,4-diketones is first reported. The ionic liquid can be recovered and reused for subsequent runs without any appreciable loss of efficiency.

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