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35982-84-4

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35982-84-4 Usage

Structure

A quinolinone ring with a hydroxymethyl and a methyl group attached

Appearance

White to off-white solid

Derivative of

Quinolinone

Common uses

Synthesis of pharmaceuticals

Potential applications

Development of new drugs

Reasons for interest

Unique structure and properties, potential biological activities

Field of research

Medicinal chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 35982-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,9,8 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 35982-84:
(7*3)+(6*5)+(5*9)+(4*8)+(3*2)+(2*8)+(1*4)=154
154 % 10 = 4
So 35982-84-4 is a valid CAS Registry Number.

35982-84-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxymethyl-1-methylquinolin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 4-Hydroxymethyl-1-methyl-1H-chinolin-2-on

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:35982-84-4 SDS

35982-84-4Downstream Products

35982-84-4Relevant articles and documents

-

Cook,Stamper

, p. 1467 (1947)

-

Light-induced cleavage of model phenylalanine conjugates based on coumarins and quinolones

Fonseca, Andrea S. C.,Goncalves, M. Sameiro T.,Costa, Susana P G.

experimental part, p. 699 - 712 (2010/12/18)

In order to evaluate the application of quinolone as a new photocleavable protecting group, in comparison with coumarin, a series of model phenylalanine conjugates were prepared by reaction with chloromethylated O and N heterocycles. The photophysical pro

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