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α-Carbomethoxy-β-(m-nitro-phenyl)-γ-nitro-buttersaeuremethylester is a complex organic compound with the chemical formula C12H12N2O8. It is a derivative of butyric acid, featuring a carbomethoxy group (ester) at the α-position, a m-nitrophenyl group at the β-position, and a nitro group at the γ-position. α-Carbomethoxy-β-(m-nitro-phenyl)-γ-nitro-buttersaeuremethylester is characterized by its ester functionality and the presence of two nitro groups, which contribute to its reactivity and potential applications in chemical research and synthesis. The compound's structure allows for various chemical transformations, making it a valuable intermediate in the preparation of other organic molecules.

22975-22-0

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22975-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22975-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,9,7 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22975-22:
(7*2)+(6*2)+(5*9)+(4*7)+(3*5)+(2*2)+(1*2)=120
120 % 10 = 0
So 22975-22-0 is a valid CAS Registry Number.

22975-22-0Relevant academic research and scientific papers

Divergent Reactivity of Nitrocyclopropanes with Huisgen Zwitterions and Facile Syntheses of 3-Alkoxy Pyrazolines and Pyrazoles

Yang, Changjiang,Liu, Wei,He, Zijian,He, Zhengjie

, p. 4936 - 4939 (2016)

A novel annulation reaction of trans-2-substituted-3-nitrocyclopropane-1,1-carboxylates with in situ generated Huisgen zwitterions is reported, providing facile synthesis of 3-alkoxy pyrazolines in good yields and high diastereoselectivities. This reactio

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