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112697-61-7

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112697-61-7 Usage

Chemical Class

Naphthyridine carboxamide

Biological Activity

Diverse range of activities, not extensively studied

Potential Pharmaceutical Applications

Medicinal chemistry

Structural Features

Methyl and phenyl groups on the nitrogen atom of the carboxamide moiety

Importance

Interesting target for further research and development due to potential influence on biological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 112697-61-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,9 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 112697-61:
(8*1)+(7*1)+(6*2)+(5*6)+(4*9)+(3*7)+(2*6)+(1*1)=127
127 % 10 = 7
So 112697-61-7 is a valid CAS Registry Number.

112697-61-7SDS

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-Methyl-N-phenyl-1,8-naphthyridine-3-carboxamide

1.2 Other means of identification

Product number -
Other names 3,5-Nonanedione,2-methyl

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:112697-61-7 SDS

112697-61-7Relevant articles and documents

Indium(Iii) Chloride as an efficient catalyst for friedlander synthesis 1,8-Naphthyridines under solventfree conditions

Mogilaiah,Manasa,Babu, H. Ramesh

, p. 209 - 212 (2019/01/18)

InCl3 catalyzed Friedlander condensation of 2-aminonicotinaldehyde 1 with carbonyl compounds containing methylene group 2 has been achieved in solvent-free grinding conditions to give 1,8-naphthyridines 3 in high yields. The method is simple an

Cecl3.7H2O catalyzed Friedlander synthesis of 1,8-naphthyridines under solvent-free grinding conditions

Mogilaiah,Kumara Swamy,Jyothi,Kavitha

, p. 305 - 308 (2019/01/21)

CeCl3.7H2O catalyses the Friedlander condensation of 2-aminonicotinaldehyde 1 with varius carbonyl compounds containing α-methylene group 2 in solvent-free grinding conditions to afford the corresponding 1,8-naphthyridines 3. The rea

An efficient Friedlander condensation using Zr(OH)2CO 3.ZrO2 as catalyst in the solid state

Mogilaiah,Swamy, T Kumara,Chandra, A Vinay

experimental part, p. 748 - 750 (2011/06/27)

A simple and efficient Friedlander condensation of 2-aminonicotinaldehyde 1 with various carbonyl compounds containing α- methylene group 2 under solid state conditions to prepare 1,8- naphthyridines 3 in very good yields using Zr(OH)2CO3

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