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Dibenzo[b,h][1,6]naphthyridine is a heterocyclic organic compound with the molecular formula C17H11N. It is a tricyclic aromatic compound consisting of two benzene rings fused to a naphthyridine ring, which is a seven-membered ring containing one nitrogen atom. Dibenzo[b,h][1,6]naphthyridine is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and properties. Dibenzo[b,h][1,6]naphthyridine can be synthesized through various methods, including condensation reactions and cyclization processes. Its chemical properties include stability, low reactivity, and the ability to form complexes with metal ions, making it a valuable building block in the development of new compounds with specific therapeutic or pesticidal activities.

225-54-7

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225-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 225-54-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,2 and 5 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 225-54:
(5*2)+(4*2)+(3*5)+(2*5)+(1*4)=47
47 % 10 = 7
So 225-54-7 is a valid CAS Registry Number.

225-54-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name quinolino[4,3-b]quinoline

1.2 Other means of identification

Product number -
Other names Dibenzo<b,h><1,6>naphthyridin

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:225-54-7 SDS

225-54-7Downstream Products

225-54-7Relevant academic research and scientific papers

Ligand-free palladium-catalyzed facile construction of tetra cyclic dibenzo[b,h][1,6]naphthyridine derivatives: Domino sequence of intramolecular C-H bond arylation and oxidation reactions

Singh, Jay Bahadur,Chandra Bharadwaj, Kishor,Gupta, Tanu,Singh, Radhey M.

, p. 26993 - 26999 (2016/03/25)

A ligand-free Pd-catalyzed approach has been developed for the synthesis of dibenzo-fused naphthyridines. The reaction involves a one-pot domino sequence of reactions involving C-H functionalisation and oxidation. The reaction was applicable to a wide range of substrates, giving the required product. Further fluorescence studies were performed where the Stoke's shift was found to be dependent on the polarity of the solvent.

Synthesis, characterization and antimicrobial activities of fused 1,6-naphthyridines

Suresh,Dhanabal,Nandha Kumar,Mohan

, p. 2375 - 2379 (2007/10/03)

An easy two-steps synthesis of 1,6-naphthyridines (4a-c, 7a-c, 10a-c, 14a-c) has been arrived from 3-formylquinolin-2(1H)-ones 1a-c and respective arylamines (2, 5, 8, 12) which underwent condensation and aromatized by dehydration with the help of PPA. All the synthesized compounds have been biologically screened for their antibacterial and antifungal activities.

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