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2-Quinoxalinecarboxamide is an organic compound with the chemical formula C9H7N3O. It is a derivative of quinoxaline, a fused bicyclic ring system consisting of a benzene ring and a pyrazine ring. This white crystalline solid is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other chemical products. 2-Quinoxalinecarboxamide exhibits a range of biological activities, including antibacterial, antifungal, and antiviral properties, making it a valuable compound in the development of new drugs and treatments. Its chemical structure and properties also make it a potential candidate for further research and development in the field of materials science and chemical engineering.

5182-90-1

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5182-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5182-90-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,8 and 2 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5182-90:
(6*5)+(5*1)+(4*8)+(3*2)+(2*9)+(1*0)=91
91 % 10 = 1
So 5182-90-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H7N3O/c10-9(13)8-5-11-6-3-1-2-4-7(6)12-8/h1-5H,(H2,10,13)

5182-90-1SDS

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 quinoxaline-2-carboxamide

1.2 Other means of identification

Product number -
Other names QUI

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:5182-90-1 SDS

5182-90-1Downstream Products

5182-90-1Relevant academic research and scientific papers

Azole-N-acetonitriles as carbonyl synthons: A one-pot preparation of heteroaryl amides from halides

Zhang, Zhongxing,Yin, Zhiwei,Kadow, John F.,Meanwell, Nicholas A.,Wang, Tao

, p. 2323 - 2326 (2007/10/03)

Azole-N-acetonitrile derivatives were utilized as synthons for an ambident carbonyl moiety via a strategy relying upon sequential base-mediated S NAr substitution of a 2-halo heterocycle, in situ oxidation, and amine displacement. This strategy allows prompt and efficient synthesis of N-containing heteroaryl amides directly from the corresponding halides via a one-pot process.

Polycyclic N-Hetero Compounds. XXII. . Reaction of Pyridine N-oxides and Pyrazino Di-N-Oxides with Formamide

Hirota, Takashi,Namba, Tetsuto,Sasaki, Kenji

, p. 949 - 953 (2007/10/02)

Reactions of pyridine N-oxides, pyrazine N-oxides and their benzologues with formamide are described.Carbamoylation mainly occured at aromatic ring with loss of the N-oxide oxygen atom, however, 2,4,6-trimethylpyridine 1-oxide gave 2- and 4-pyrimidinyl derivatives.

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