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40296-15-9

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40296-15-9 Usage

Synthesis

Formed by the reaction of 2-acetylbenzoic acid and benzoyl chloride to produce a triester.

Common Uses

Plasticizer: Added to polymers to enhance flexibility and durability.
Perfumes: Used in the production of fragrances.
Pharmaceuticals: Incorporated into pharmaceutical products.
Industrial Products: Utilized in various industrial applications.

Physical Properties

Appearance: White to off-white crystalline powder.
Melting Point: High melting point, suitable for industrial processes.

Toxicity

Relatively low toxicity.

Environmental Impact

Not considered a significant environmental hazard.

Check Digit Verification of cas no

The CAS Registry Mumber 40296-15-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,2,9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40296-15:
(7*4)+(6*0)+(5*2)+(4*9)+(3*6)+(2*1)+(1*5)=99
99 % 10 = 9
So 40296-15-9 is a valid CAS Registry Number.

40296-15-9SDS

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-acetyl-3,5-dibenzoyloxyphenyl) benzoate

1.2 Other means of identification

Product number -
Other names Ethanone, 1-[2,4,6-tris(benzoyloxy)phenyl]-

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:40296-15-9 SDS

40296-15-9Relevant articles and documents

Baker-venkataraman rearrangement under microwave irradiation: A new strategy for the synthesis of 3-aroyl-5-hydroxyflavones

Pinto, Diana C. G. A.,Silva, Artur M. S.,Cavaleiro, José A. S.

, p. 1897 - 1900 (2008/03/13)

Microwave irradiation selectively induces the Baker-Venkataraman rearrangement of 2′,6′-diaroyloxyacetophenones to give 3-aroyl-5-hydroxyflavones, in a very short reaction time. Under classical heating conditions these reactions afforded 5-hydroxyflavones

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