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42712-44-7

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42712-44-7 Usage

Derivative

It is a derivative of quinoline.

Functional Groups

Amino Group: Contains an amino group.
Hydroxy Group: Contains a hydroxy group.
Methyl Group: Attached to the quinoline ring.

Pharmacological and Biological Activities

Anti-malarial Agent: Investigated for its potential role as an anti-malarial agent.
Fluorescent Dye: Studied for its potential use as a fluorescent dye for labeling biomolecules in biological research.
Antioxidant Properties: Studied for potential antioxidant properties.
Anti-inflammatory Properties: Investigated for potential anti-inflammatory properties.

Check Digit Verification of cas no

The CAS Registry Mumber 42712-44-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,7,1 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 42712-44:
(7*4)+(6*2)+(5*7)+(4*1)+(3*2)+(2*4)+(1*4)=97
97 % 10 = 7
So 42712-44-7 is a valid CAS Registry Number.

42712-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-6-methyl-1H-quinolin-4-one

1.2 Other means of identification

Product number -
Other names 2-Amino-4-hydroxy-6-methylquinoline

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:42712-44-7 SDS

42712-44-7Downstream Products

42712-44-7Relevant articles and documents

-

Kadin,Lamphere

, p. 500 (1977)

-

2-Amino-3-cyano-4-hydroxyquinolines

-

, (2008/06/13)

The reaction of isatoic anhydrides with malononitrile in a reaction-inert solvent in the presence of a base to produce 2-amino-3-cyano-4-hydroxyquinolines and 2-amino-α,α-dicyanoacetophenones which are then hydrolyzed and decarboxylated under acid or base conditions to produce 2-amino-4-hydroxyquinolines, useful as intermediates for preparation of 1-oxo-1H-6-alkoxypyrimido[1,2-a]quinoline-2-carboxylic acids and esters of value as antiallergy agents.

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