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61522-57-4

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61522-57-4 Usage

General Description

Ethanone, 1-(3-methyl-1-oxido-2-quinoxalinyl)- is a chemical compound that contains a quinoxaline ring and a ketone functional group. Its molecular structure includes a methyl group attached to the quinoxaline ring and an oxido group attached to the aromatic nitrogen of the ring. Ethanone, 1-(3-methyl-1-oxido-2-quinoxalinyl)- is used in various industrial applications, such as in the synthesis of pharmaceuticals and agrochemicals. It may also have potential biological activities, although further research is needed to fully understand its properties and potential uses. Overall, Ethanone, 1-(3-methyl-1-oxido-2-quinoxalinyl)- is a versatile chemical compound with a unique structure that offers possibilities for diverse applications.

Check Digit Verification of cas no

The CAS Registry Mumber 61522-57-4 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 61522-57:
(7*6)+(6*1)+(5*5)+(4*2)+(3*2)+(2*5)+(1*7)=104
104 % 10 = 4
So 61522-57-4 is a valid CAS Registry Number.

61522-57-4Downstream Products

61522-57-4Relevant 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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