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9-oxo-1,2,3,9-tetrahydro-4H-cyclopenta[b]quinoxalin-9-ium-4-olate is a complex organic compound with the molecular formula C11H10N2O2. It is a derivative of cyclopenta[b]quinoxaline, a heterocyclic aromatic compound consisting of a cyclopentane ring fused to a quinoxaline ring. The compound features a 9-oxo group, indicating the presence of a carbonyl group at the 9-position, and a 4-olate group, which is a negatively charged oxygen atom at the 4-position. This chemical structure is significant in the field of organic chemistry and may have potential applications in pharmaceuticals or materials science due to its unique properties and reactivity. However, further research and characterization are needed to fully understand its potential uses and effects.

4232-53-5

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4232-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4232-53-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4232-53:
(6*4)+(5*2)+(4*3)+(3*2)+(2*5)+(1*3)=65
65 % 10 = 5
So 4232-53-5 is a valid CAS Registry Number.

4232-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-oxido-2,3-dihydro-1H-cyclopenta[b]quinoxalin-4-ium 4-oxide

1.2 Other means of identification

Product number -
Other names 2,3-Dihydro-1H-cyclopenta<b>chinoxalin-N,N'-dioxid

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:4232-53-5 SDS

4232-53-5Downstream Products

4232-53-5Relevant academic research and scientific papers

Unusual friedlander reactions: A route to novel quinoxaline-based heterocycles

Shoker, Tharallah A.,Ghattass, Khaled I.,Fettinger, James C.,Kurth, Mark J.,Haddadin, Makhluf J.

supporting information; experimental part, p. 3704 - 3707 (2012/09/21)

Acid catalyzed Friedlander reactions of a number of 2,3-dihydro-1H- cyclopenta[b]quinoxaline-1-ones with 2-aminobenzaldehyde yield, unexpectedly, 8H-indolo[3,2-a]phenazine and quinolino[2,3-c]cyclopentadienone[2,3-b] quinoxalines, the structures of derivatives of which were confirmed by X-ray crystallography. Easy routes to novel quinoxaline-based indoles, quinolones, and quinoxaline-1,4-dioxides are reported, and proposed mechanisms for the unexpected products are discussed.

Quinoxaline derivatives

-

, (2008/06/13)

The synthesis of quinoxaline and benzimidazole-N-oxides and of ester and amide derivatives of 3-hydroxy-2-quinoxalinecarboxylic acid by a novel process consisting of the reaction between a benzofuroxan and an activated methylene-containing compound under basic conditions.

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