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1,5-Pentanediol, acetate 4-methylbenzenesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26923-85-3

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26923-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26923-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,9,2 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26923-85:
(7*2)+(6*6)+(5*9)+(4*2)+(3*3)+(2*8)+(1*5)=133
133 % 10 = 3
So 26923-85-3 is a valid CAS Registry Number.

26923-85-3SDS

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 acetic acid,4-methylbenzenesulfonic acid,pentane-1,5-diol

1.2 Other means of identification

Product number -
Other names 1,5-Pentanediol,acetate 4-methylbenzenesulfonate

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:26923-85-3 SDS

26923-85-3Downstream Products

26923-85-3Relevant academic research and scientific papers

Polystyrene-supported GaCl3: A new, highly efficient and recyclable heterogeneous Lewis acid catalyst for acetylation and benzoylation of alcohols and phenols

Rahmatpour, Ali

, p. 1048 - 1054 (2012)

A new, simple and highly chemoselective method for both acetylation and benzoylation of alcohols and phenols with acetic anhydride in the presence of polystyrene-supported gallium trichloride (PS/GaCl3) as a highly active and reusable heterogeneous Lewis acid catalyst is presented. In this catalytic system, primary, secondary and tertiary alcohols as well as phenols were converted to the corresponding acetates and benzoates with high yields. The heterogenized catalyst is of high reusability and stability in the acetylation reactions and was recovered several times with negligible loss in its activity or a negligible catalyst leaching, and also there is no need for regeneration. Remarkably, a selective mono-acetylation of symmetrical diols can be achieved chemoselectively by employing the same catalyst.

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