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4-Azidoquinoline 1-oxide is a chemical compound with the molecular formula C9H6N4O and a molecular weight of 182.17 g/mol. It is a derivative of quinoline, a heterocyclic aromatic compound, and features an azide group (N3) attached to the 4-position of the quinoline ring. 4-azidoquinoline 1-oxide is known for its potential use in the synthesis of various pharmaceuticals and agrochemicals, as well as in the preparation of fluorescent probes and other functional materials. Due to the presence of the azide group, 4-azidoquinoline 1-oxide can undergo a variety of chemical reactions, such as click chemistry, which allows for the formation of stable triazole linkages with alkynes. This property makes it a valuable building block in the development of new compounds with specific biological activities or material properties.

2669-36-5

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2669-36-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2669-36-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,6 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2669-36:
(6*2)+(5*6)+(4*6)+(3*9)+(2*3)+(1*6)=105
105 % 10 = 5
So 2669-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H6N4O/c10-12-11-8-5-6-13(14)9-4-2-1-3-7(8)9/h1-6H

2669-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-azido-1-oxidoquinolin-1-ium

1.2 Other means of identification

Product number -
Other names Quinoline,4-azido-,1-oxide

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:2669-36-5 SDS

2669-36-5Upstream product

2669-36-5Relevant academic research and scientific papers

4-Azidoquinoline N-oxide: Synthesis and photolysis

Shaforost,Ryzhakov,Rodina

experimental part, p. 728 - 730 (2009/04/07)

In photolysis of 4-azidoquinoline N-oxide azoxy compound was isolated as the final reaction product. This result may be ascribed to the dimerization of the intermediate nitrene to azo compound followed by oxidation of the latter with air oxygen. The initially arising nitrene is stabilized by resonance conjugation involving the aromatic system and the N-oxide group. The rate constants of 4-azidoquinoline N-oxide photolysis were measured in various solvents and the values of spin density and bond lengths in the formed nitrene were calculated.

Reaction of 4-azidoquinoline N-oxide with dimethyl acetylenedicarboxylate

Ryzhakov,Rodina

, p. 700 - 701 (2007/10/03)

The reaction of 4-azidoquinoline N-oxide with dimethyl acetylenedicarboxylate occurs via a 1,3-dipolar cycloaddition mechanism at the N-oxide and not at the azide group.

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