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4-Hydroxy-6-nitro-1,8-naphthyridine-3-carbonitrile is a chemical compound with the molecular formula C9H4N4O3. It is a derivative of 1,8-naphthyridine, a heterocyclic compound consisting of a fused pyridine and pyrimidine ring system. This specific compound features a hydroxyl group (-OH) at the 4-position, a nitro group (-NO2) at the 6-position, and a cyano group (-CN) at the 3-position. It is an organic molecule with potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound is known for its stability and can be used as an intermediate in the preparation of other complex molecules. Its properties, such as solubility and reactivity, can be influenced by the presence of these functional groups, making it a versatile building block in organic synthesis.

690223-99-5

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690223-99-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 690223-99-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,0,2,2 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 690223-99:
(8*6)+(7*9)+(6*0)+(5*2)+(4*2)+(3*3)+(2*9)+(1*9)=165
165 % 10 = 5
So 690223-99-5 is a valid CAS Registry Number.

690223-99-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names -

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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:690223-99-5 SDS

690223-99-5Relevant 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 (2004)

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.

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