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4-Chloro-6-nitro-1,8-naphthyridine-3-carbonitrile is a chemical compound with the molecular formula C10H4ClN3O2. It is a naphthyridine derivative characterized by the presence of a chlorine atom at position 4, a nitro group at position 6, and a cyano group at position 3. 4-chloro-6-nitro-1,8-naphthyridine-3-carbonitrile possesses potential applications in various fields due to its unique chemical structure and properties.

305370-84-7

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305370-84-7 Usage

Uses

Used in Pharmaceutical Industry:
4-Chloro-6-nitro-1,8-naphthyridine-3-carbonitrile is used as an active pharmaceutical ingredient for its antibacterial and antifungal properties. Its ability to inhibit the growth of harmful microorganisms makes it a valuable compound in the development of new drugs to combat resistant infections.
Used in Synthesis of Heterocyclic Compounds:
This naphthyridine derivative is utilized as a key intermediate in the synthesis of various heterocyclic compounds. Its unique structure allows for the formation of diverse chemical entities with potential applications in different industries.
Used in Drug Development:
4-Chloro-6-nitro-1,8-naphthyridine-3-carbonitrile serves as a building block in the development of new drugs. Its chemical properties enable the creation of novel therapeutic agents with improved efficacy and selectivity.
Used as a Dye Intermediate:
In the dye industry, 4-chloro-6-nitro-1,8-naphthyridine-3-carbonitrile is used as an intermediate in the production of various dyes. Its chemical structure contributes to the color and stability of the resulting dyes.
Used in Organic Synthesis Processes:
4-chloro-6-nitro-1,8-naphthyridine-3-carbonitrile is employed in various organic synthesis processes due to its reactivity and functional groups. It can be used to synthesize a wide range of organic compounds for different applications, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 305370-84-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,5,3,7 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 305370-84:
(8*3)+(7*0)+(6*5)+(5*3)+(4*7)+(3*0)+(2*8)+(1*4)=117
117 % 10 = 7
So 305370-84-7 is a valid CAS Registry Number.

305370-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-chloro-6-nitro-1,8-naphthyridine-3-carbonitrile

1.2 Other means of identification

Product number -
Other names 1,8-NAPHTHYRIDINE-3-CARBONITRILE,4-CHLORO-6-NITRO

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:305370-84-7 SDS

305370-84-7Relevant academic research and scientific papers

Syntheses and EGFR kinase inhibitory activity of 6-substituted-4-anilino [1,7] and [1,8] naphthyridine-3-carbonitriles

Wissner, Allan,Hamann, Philip R.,Nilakantan, Ramaswamy,Greenberger, Lee M.,Ye, Fei,Rapuano, Timothy A.,Loganzo, Frank

, p. 1411 - 1416 (2007/10/03)

The syntheses and EGFR kinase inhibitory activity of a series of 6-substituted-4-anilino [1,7] and [1,8] naphthyridine-3-carbonitriles are described. Both reversible and irreversible binding inhibitors were prepared. These series were compared with each other and with the corresponding 4-anilinoquinoline-3-carbonitriles. Compounds having a 1,7-naphthyridine core structure can retain high potency while those with a 1,8-naphthyridine core are significantly less active. These results are consistent with molecular modeling observations.

SUBSTITUTED-3-CYANO-[1.7],[1.5], AND [1.8]-NAPHTHYRIDINE INHIBITORS OF TYROSINE KINASES

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Page 47, (2010/02/06)

This invention provides compounds of formula (I) having structure (a) wherein A'' is a diavalent moiety selected from the group (a, b, c) which are useful as inhibitors of protein tyrosine kinase.

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