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1,8-Naphthyridine-2,7-diamine, N-(phenylmethyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

898258-05-4

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898258-05-4 Usage

Derivative of naphthyridine

Yes
It is derived from the organic compound naphthyridine, which is a type of fused heterocyclic compound.

Contains a phenylmethyl group

Yes
The compound has a phenylmethyl group attached to it, which is a benzene ring with a methyl group.

Potential applications

Pharmaceuticals
It has potential uses in the pharmaceutical industry due to its medicinal properties.

Medicinal properties

Under investigation
The specific medicinal properties and effects of 1,8-Naphthyridine-2,7-diamine, N-(phenylmethyl)- (9CI) are still being studied and researched.

Drug development

Being studied
The compound is being investigated for its potential use in drug development, but further research and testing are needed to determine its full range of applications and effects.

Further research and testing

Required
Additional research and testing are necessary to fully understand the potential applications and effects of 1,8-Naphthyridine-2,7-diamine, N-(phenylmethyl)- (9CI) in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 898258-05-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,8,2,5 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 898258-05:
(8*8)+(7*9)+(6*8)+(5*2)+(4*5)+(3*8)+(2*0)+(1*5)=234
234 % 10 = 4
So 898258-05-4 is a valid CAS Registry Number.

898258-05-4Downstream Products

898258-05-4Relevant academic research and scientific papers

Simple and efficient synthesis of 2,7-difunctionalized-1,8-naphthyridines

Goswami, Shyamaprosad,Mukherjee, Reshmi,Mukherjee, Rakhi,Jana, Subrata,Maity, Annada C.,Adak, Avijit Kumar

, p. 929 - 936 (2007/10/03)

The syntheses in good yields of some new difunctionalized 1,8-naphthyridines 4, 6, 8 and 9 and a novel triethylene glycol ether-linked dinaphthyridine, 10a, along with the mononaphthyridine-linked ether alcohol 10b are described. An improved and milder method for the synthesis of 2,7-diamino-1,8-naphthyridine (14) is also reported.

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