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6-Nitroimino-5α-cholestane is a chemical compound derived from the parent steroid molecule, cholestane. It is characterized by the presence of a nitroimino group (-N=NO2) at the 6th position and a 5α-configuration, which refers to the stereochemistry of the molecule. 6-nitroimino-5α-cholestane is of interest in the field of organic chemistry, particularly in the study of steroidal compounds and their potential applications in pharmaceuticals and other industries. The nitro group's presence can significantly alter the compound's reactivity and properties compared to its parent cholestane, making it a subject of research for its unique chemical behavior and potential therapeutic uses.

2735-32-2

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2735-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2735-32-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2735-32:
(6*2)+(5*7)+(4*3)+(3*5)+(2*3)+(1*2)=82
82 % 10 = 2
So 2735-32-2 is a valid CAS Registry Number.

2735-32-2Relevant academic research and scientific papers

N-Nitrosation of Some Steroidal 6-Ketoximes

Ahmad, M. S.,Raza, S. K.

, p. 774 - 775 (2007/10/02)

Steroidal 6-nitrimines, namely 6-nitrimino-5α-cholestane (IV) and its 3β-acetoxy (V) and 3β-chloro (VI) analogues have been obtained by the N-nitrosation of the respective oximes (I-III).The nitrimines (IV-VI) on alkali isomerization give N-nitroenamines (X-XII).NaBH4 reduction of IV-VI affords the respective nitroamines (XIII-XV).The products have been characterized on the basis of their spectral and analytical data and chemical transformations.

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