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Pyrrolo[1,2-a]quinoxaline, 4-methylis a chemical compound belonging to the pyrroloquinoxaline class of organic compounds. It features a fused ring system consisting of a pyrrole and a quinoxaline ring, with a methyl group attached at the 4-position of the pyrrole ring. This unique structure endows it with potential applications in chemical and pharmaceutical industries, as well as in pharmaceutical research and development.

1931-32-4

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1931-32-4 Usage

Uses

Used in Pharmaceutical Research and Development:
Pyrrolo[1,2-a]quinoxaline, 4-methylis utilized as a research compound for exploring its potential biological activity and pharmaceutical relevance. Its unique structural properties make it a candidate for the development of new drugs and therapeutic agents.
Used in Organic Synthesis:
In the chemical industry, Pyrrolo[1,2-a]quinoxaline, 4-methylserves as a key intermediate in the synthesis of various organic compounds. Its presence in the synthesis process can lead to the creation of new compounds with potential applications in different fields, including pharmaceuticals, agrochemicals, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 1931-32-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 1 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1931-32:
(6*1)+(5*9)+(4*3)+(3*1)+(2*3)+(1*2)=74
74 % 10 = 4
So 1931-32-4 is a valid CAS Registry Number.

1931-32-4Upstream product

1931-32-4Relevant academic research and scientific papers

Iron-Catalyzed Intramolecular C(sp2)-N Cyclization of 1-(N-Arylpyrrol-2-yl)ethanone O-Acetyl Oximes toward Pyrrolo[1,2-a]quinoxaline Derivatives

Zhang, Zhiguo,Li, Junlong,Zhang, Guisheng,Ma, Nana,Liu, Qingfeng,Liu, Tongxin

, p. 6875 - 6884 (2015)

An efficient and convenient iron-catalyzed protocol has been developed for the synthesis of substituted pyrrolo[1,2-a]quinoxalines from 1-(N-arylpyrrol-2-yl)ethanone O-acetyl oximes through N-O bond cleavage and intramolecular directed C-H arylation reactions in acetic acid.

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