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61522-56-3

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61522-56-3 Usage

General Description

Ethanone, 1-(3-methyl-4-oxido-2-quinoxalinyl)-, also known as quinoxalin-2(1H)-one-3-methyl-4-oxide, is a chemical compound that belongs to the quinoxaline class of organic compounds. It is a yellow crystalline solid with a molecular formula C11H10N2O2 and a molecular weight of 198.21 g/mol. Ethanone, 1-(3-methyl-4-oxido-2-quinoxalinyl)- is a derivative of quinoxaline and is known for its potential pharmacological properties, such as anti-inflammatory and analgesic activities. Its structure includes a quinoxaline ring with an additional methyl group and an oxido group attached, giving it unique chemical properties that make it suitable for various pharmaceutical and medicinal applications.

Check Digit Verification of cas no

The CAS Registry Mumber 61522-56-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,2 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 61522-56:
(7*6)+(6*1)+(5*5)+(4*2)+(3*2)+(2*5)+(1*6)=103
103 % 10 = 3
So 61522-56-3 is a valid CAS Registry Number.

61522-56-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-methyl-4-oxidoquinoxalin-4-ium-2-yl)ethanone

1.2 Other means of identification

Product number -
Other names 1-deoxymequindox

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:61522-56-3 SDS

61522-56-3Relevant articles and documents

REACTIONS OF 2-ACETYL-3-METHYLQUINOXALINE 1,4-DIOXIDE AND ITS DERIVATIVES

Matoba, Katsuhide,Terada, Takashi,Sugiura, Masaru

, p. 55 - 58 (2007/10/02)

2-Cinnamoyl-3-methylquinoxaline 1,4-dioxide (2) was inert to hydrochloric acid in refluxing ethanol.When a xylene solution of 2-acetyl-3-methylquinoxaline 1,4-dioxide (1-dioxide) was refluxed overnight, the dioxide was reduced mainly to 1,4-oxide and the oxidative products from xylene were also obtained. 2-Cinnamoyl-3-methylquinoxaline 4-oxide (4a) and 3-methyl-4-oxido-2-quinoxalyl 4-phenyl-1,3-butadienyl ketone (4b) were quantitatively cyclized into 4-methyl-3-oxo-1-phenyl- and 4-methyl-3-oxo-1-styryl-3H-pyrroloquinoxalin-10-ium chloride (6a and 6 b), respectively , when the ethanolic solution were refluxed in the presence of hydrochloric acid.

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