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2H-1-Benzopyran-2-one, 3-(4-bromophenyl)-4-hydroxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62497-36-3

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62497-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62497-36-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,4,9 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62497-36:
(7*6)+(6*2)+(5*4)+(4*9)+(3*7)+(2*3)+(1*6)=143
143 % 10 = 3
So 62497-36-3 is a valid CAS Registry Number.

62497-36-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-bromophenyl)-4-hydroxychromen-2-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:62497-36-3 SDS

62497-36-3Downstream Products

62497-36-3Relevant academic research and scientific papers

Coumestan inhibits radical-induced oxidation of DNA: Is hydroxyl a necessary functional group?

Xi, Gao-Lei,Liu, Zai-Qun

, p. 5636 - 5642 (2014/07/07)

Coumestan is a natural tetracycle with a C - C bond shared by a coumarin moiety and a benzofuran moiety. In addition to the function of the hydroxyl group on the antioxidant activity of coumestan, it is worth exploring the influence of the oxygen-abundant

Coumestan inhibits radical-induced oxidation of dna: Is hydroxyl a necessary functional groupΔ

Xi, Gao-Lei,Liu, Zai-Qun

, p. 5636 - 5642 (2015/04/22)

Coumestan is a natural tetracycle with a C=C bond shared by a coumarin moiety and a benzofuran moiety. In addition to the function of the hydroxyl group on the antioxidant activity of coumestan, it is worth exploring the influence of the oxygen-abundant s

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