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81398-31-4

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81398-31-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81398-31-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,9 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81398-31:
(7*8)+(6*1)+(5*3)+(4*9)+(3*8)+(2*3)+(1*1)=144
144 % 10 = 4
So 81398-31-4 is a valid CAS Registry Number.

81398-31-4SDS

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 (S)-5,7-Dihydroxy-2-(3,4,5-trihydroxy-phenyl)-chroman-4-one

1.2 Other means of identification

Product number -
Other names -

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:81398-31-4 SDS

81398-31-4Relevant articles and documents

Synthesis and biological evaluation of 5,7-dihydroxyflavanone derivatives as antimicrobial agents

Zhang, Xing,Khalidi, Omar,Kim, So Young,Wang, Ruitong,Schultz, Victor,Cress, Brady F.,Gross, Richard A.,Koffas, Mattheos A.G.,Linhardt, Robert J.

, p. 3089 - 3092 (2016/06/13)

A series of 5,7-dihydroxyflavanone derivatives were efficiently synthesized. Their antimicrobial efficacy on Gram-negative, Gram-positive bacteria and yeast were evaluated. Among these compounds, most of the halogenated derivatives exhibited the best antimicrobial activity against Gram-positive bacteria, the yeast Saccharomyces cerevisiae, and the Gram-negative bacterium Vibrio cholerae. The cytotoxicities of these compounds were low as evaluated on HepG2 cells using a cell viability assay. This study suggests that halogenated flavanones might represent promising pharmacological candidates for further drug development.

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