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2-Naphthalenecarboxylic acid, 4-methylphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88639-90-1

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88639-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88639-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,6,3 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88639-90:
(7*8)+(6*8)+(5*6)+(4*3)+(3*9)+(2*9)+(1*0)=191
191 % 10 = 1
So 88639-90-1 is a valid CAS Registry Number.

88639-90-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylphenyl) naphthalene-2-carboxylate

1.2 Other means of identification

Product number -
Other names 2-Naphthalenecarboxylic acid,4-methylphenyl 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:88639-90-1 SDS

88639-90-1Relevant articles and documents

Electrodimerization of N-Alkoxyamides for Zinc(II) Catalyzed Phenolic Ester Synthesis under Mild Reaction Conditions

Subramanian, Kripa,Yedage, Subhash L.,Bhanage, Bhalchandra M.

, p. 2511 - 2521 (2018/05/14)

An electrochemical On-Off method for phenolic ester synthesis from N-alkoxyamides has been reported. This one-pot protocol begins with rapid and selective electrodimerization of the amide using n-Bu4NI (TBAI) as an electrocatalyst. The reaction proceeds further in the absence of current via Zn catalyzed C?N bond activation of the amide dimer followed by its coupling with phenol to form the ester. The present methodology is ligand-free and takes place under mild reaction conditions. This transformation incorporates a wide variety of phenols and amide substrates leading to the formation of functionalized esters highlighting its versatility. (Figure presented.).

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