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307524-67-0

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307524-67-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 307524-67-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,7,5,2 and 4 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 307524-67:
(8*3)+(7*0)+(6*7)+(5*5)+(4*2)+(3*4)+(2*6)+(1*7)=130
130 % 10 = 0
So 307524-67-0 is a valid CAS Registry Number.

307524-67-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-oxo-N-(2-phenylethyl)chromene-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3-carboxamido coumarin,37

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:307524-67-0 SDS

307524-67-0Downstream Products

307524-67-0Relevant articles and documents

Design and synthesis of coumarin-3-acylamino derivatives to scavenge radicals and to protect DNA

Yang, Yang,Liu, Qing-Wen,Shi, Ye,Song, Zhi-Guang,Jin, Ying-Hua,Liu, Zai-Qun

, p. 1 - 7 (2014/07/22)

In this study, a series of coumarin-3-acylamino derivatives containing phenethylamine moiety or tyramine moiety were synthesized and their antioxidant activities were evaluated by Cu2+/glutathione(GSH)-, OH- and 2,2′-azobis(2-amidinopropane hyd

Synthesis of novel 3-substitued coumarin carboxamides with biological interest and their spectral studies

Das, Asish R.,Medda, Arunima,Singha, Raghunath,Samanta, Anuva,Guchhait, Nikhil

experimental part, p. 1124 - 1129 (2010/03/03)

The 3-substitued coumarin carboxamides are prepared by a highly efficient one-pot procedure. The coupling reaction of coumarin carboxylic acids and its acid chlorides with different amines affodred amide derivatives of coumarin in moderate to high yields

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