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Benzo[b][1,7]naphthyridine is a heterocyclic aromatic compound consisting of a benzene ring fused to a naphthyridine ring. It is a tricyclic structure with a total of 12 carbon atoms and 5 nitrogen atoms, featuring a benzene ring attached to a 1,7-naphthyridine ring. Benzo[b][1,7]naphthyridine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties. The chemical formula for benzo[b][1,7]naphthyridine is C13H9N, and it is characterized by its stability, reactivity, and the ability to form various derivatives, making it a valuable building block in organic chemistry.

260-95-7

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260-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 260-95-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 260-95:
(5*2)+(4*6)+(3*0)+(2*9)+(1*5)=57
57 % 10 = 7
So 260-95-7 is a valid CAS Registry Number.

260-95-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[b][1,7]naphthyridine

1.2 Other means of identification

Product number -
Other names benzo<b><1,7>naphthyridine

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:260-95-7 SDS

260-95-7Downstream Products

260-95-7Relevant academic research and scientific papers

INTRAMOLECULAR NITRENE INSERTIONS INTO AROMATIC AND HETEROAROMATIC RINGS. PART 8. FLASH VACUUM PYROLYSIS OF 2-AZIDOBENZYLPYRIDINES

Hicks, Martin G.,Jones, Gurnos.,York, David C.

, p. 69 - 76 (2007/10/02)

Flash vacuum pyrolysis of 2-azidobenzylpyridines (9)-(11) at temperatures from 350 to 700 deg C gave mixtures of benzonaphthyridines and their dihydro derivatives as major products.The 3-pyridyl derivative (10) also gave 2-(3-cyanoprop-1-enyl)indole (19).Benzonaphthyridines were also obtained by pyrolysis of 2-aminophenyl(x-pyridyl)methanols (4), (5), and (6), .Treatment of the azides (9)-(11) with aluminium chloride gave the corresponding 2-amino-5-chlorobenzylpyridines (21)-(23).The mechanism of the reaction is discussed.

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