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54756-24-0

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54756-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54756-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,7,5 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 54756-24:
(7*5)+(6*4)+(5*7)+(4*5)+(3*6)+(2*2)+(1*4)=140
140 % 10 = 0
So 54756-24-0 is a valid CAS Registry Number.

54756-24-0SDS

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 2-benzoyl-2-hydroxy-1-benzofuran-3-one

1.2 Other means of identification

Product number -
Other names 2-Hydroxy-2-benzoyl-3(2H)-benzofuranon

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:54756-24-0 SDS

54756-24-0Upstream product

54756-24-0Downstream Products

54756-24-0Relevant articles and documents

Flavonoid epoxides. Part 20. Some unusual reactions of dimethyldioxirane (DMD) with flavonoid compounds

Burke, Anthony J.,O'Sullivan, W. Ivo

, p. 8491 - 8500 (2007/10/03)

Dimethyldioxirane (DMD), generally as a solution in acetone, has proved itself to be an excellent epoxidising agent. It was observed that either the 2'-hydroxychalcone epoxide or the tans-2,3-dihydroflavonol could be obtained depending on the pH of the reaction mixture and the type of β-arene ring present in the substrate. Using this methodology trans-2,3-dihydroflavonols can be synthesised in far better yields than by the most commonly used method for their synthesis, that of the Algar-Flynn-Oyamada reaction. Treatment of both flavonol 14 and the novel isoaurone 21 with DMD gave unusual products instead of the expected epoxides, but nonetheless, an epoxide was assumed to have formed during the reaction.

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