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Benzoic acid, 3,4,5-tris(acetyloxy)-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

73607-60-0

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73607-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 73607-60-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,0 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 73607-60:
(7*7)+(6*3)+(5*6)+(4*0)+(3*7)+(2*6)+(1*0)=130
130 % 10 = 0
So 73607-60-0 is a valid CAS Registry Number.

73607-60-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 3,4,5-triacetyloxybenzoate

1.2 Other means of identification

Product number -
Other names Triacetyl-gallussaeure-aethylester

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:73607-60-0 SDS

73607-60-0Downstream Products

73607-60-0Relevant academic research and scientific papers

Novel chemoselective de-esterification of esters of polyacetoxy aromatic acids by lipases

Parmar, Virinder S.,Kumar, Ajay,Bicht, Kirpal S.,Mukherjee, Shubhasish,Prasad, Ashok K.,Sharma, Sunil K.,Wengel, Jesper,Olsen, Carl E.

, p. 2163 - 2176 (2007/10/03)

Candida cylindracea lipase (CCL) and porcine pancreatic lipase (PPL) have been used for deacetylation of peracetates of methyl and ethyl esters of six different polyphenolic acids in organic solvents. Exclusive de-esterification of the ester groups derived from the phenolic hydroxy and aliphatic acid over the ester group of the aromatic acid and aliphatic alcohol has been achieved affording the corresponding esters of phenolic acids in as high yields as 90-97%. The results have been corroborated with the mechanism of lipase action.

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