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2-Amino-[1,8]Naphthyridine-3-Carbonitrile is a chemical compound that falls under the category of naphthyridines, which are polycyclic aromatic compounds. These compounds are characterized by the presence of three rings, with two of the rings sharing two common carbon atoms to form a naphthyridine moiety. In this specific compound, it features an amino group attached to the second carbon atom and a carbonitrile group attached to the third carbon atom of the naphthyridine ring. Although it has potential applications in research, chemical reactions, and pharmaceuticals, the specific uses, properties, and toxicological effects of 2-Amino-[1,8]Naphthyridine-3-Carbonitrile are not well-documented, necessitating further investigation and research.

15935-95-2

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15935-95-2 Usage

Uses

Used in Research Applications:
2-Amino-[1,8]Naphthyridine-3-Carbonitrile is used as a research chemical for the study of its properties and potential applications in various fields. Its unique structure and functional groups make it a candidate for exploration in chemical reactions and synthesis processes.
Used in Pharmaceutical Development:
2-Amino-[1,8]Naphthyridine-3-Carbonitrile is used as a starting material or intermediate in the development of pharmaceutical compounds. Its amino and carbonitrile groups can be utilized in the synthesis of new drug molecules, potentially leading to the discovery of novel therapeutic agents.
Used in Chemical Reactions:
2-Amino-[1,8]Naphthyridine-3-Carbonitrile is used as a reactant in various chemical reactions, allowing for the formation of new compounds with different properties and potential applications. Its reactivity can be explored in the context of organic synthesis and the development of new chemical methodologies.
Note: Due to the lack of universally documented information on the specific usage, properties, and toxicological effects of 2-Amino-[1,8]Naphthyridine-3-Carbonitrile, it is essential to conduct further studies to better understand its potential applications and limitations in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 15935-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,3 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15935-95:
(7*1)+(6*5)+(5*9)+(4*3)+(3*5)+(2*9)+(1*5)=132
132 % 10 = 2
So 15935-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N4/c10-5-7-4-6-2-1-3-12-9(6)13-8(7)11/h1-4H,(H2,11,12,13)

15935-95-2 Well-known Company Product Price

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  • Aldrich

  • (ADE000830)  2-Amino-[1,8]naphthyridine-3-carbonitrile  AldrichCPR

  • 15935-95-2

  • ADE000830-1G

  • 1,930.50CNY

  • Detail

15935-95-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Amino-[1,8]naphthyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 2-amino-1,8-naphthyridine-3-carbonitrile

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:15935-95-2 SDS

15935-95-2Relevant academic research and scientific papers

Microwave induced Friedlander condensation - A facile synthesis of 1,8-naphthyridines

Mogilaiah,Reddy, N. Vasudeva

, p. 215 - 217 (2007/10/03)

A simple and efficient method has been developed for the rapid synthesis of 1,8-naphthyridines 3 from 2-aminonicotinaldehyde 1 and active methylene compounds 2 in methanol in the presence of a catalytic amount of piperidine in unmodified domestic microwav

Synthesis of 1,8-naphthyridines under solvent free conditions

Mogilaiah,Rao

, p. 713 - 714 (2007/10/03)

Various active methylene compounds 2 reacts efficiently with 2-aminonicotinaldehyde 1 in the presence of piperidine at room temperature within a few minutes and furnish the corresponding 1,8-naphthyridines 3 in high yield under solvent free conditions.

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