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1711-35-9

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1711-35-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1711-35-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 1 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1711-35:
(6*1)+(5*7)+(4*1)+(3*1)+(2*3)+(1*5)=59
59 % 10 = 9
So 1711-35-9 is a valid CAS Registry Number.

1711-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methyl-benzoic acid m-tolyl ester

1.2 Other means of identification

Product number -
Other names m-Methylphenyl-p-toluat

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:1711-35-9 SDS

1711-35-9Relevant articles and documents

Study on the aromatic transesterification reaction catalyzed by phosphotungstic acid

He, Hong-Qiang,Chang, Yu-Wei,Xu, Wei-Ming

supporting information, p. 280 - 282 (2015/06/22)

A practical phosphotungstic acid-catalyzed aromatic transesterification reaction for the preparation of aryl benzoates has been developed. The transesterification method avoids the oxidation of the corresponding phenols to quinone compounds with easy operations, environmentally benign conditions and high yields of the products. It is noteworthy that in this process phosphotungstic acid can be reused and recycled.

A convenient procedure for the esterification of benzoic acids with phenols: a new application for the Mitsunobu reaction

Fitzjarrald, Victor P.,Pongdee, Rongson

, p. 3553 - 3557 (2008/02/06)

The Mitsunobu reaction was found to be a convenient and effective method for the esterification of various benzoic acids with differentially functionalized phenols producing the corresponding phenyl esters in good to excellent yields.

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