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3,5-Cyclocholestane is a cyclic hydrocarbon compound derived from cholesterol, characterized by the presence of a cyclopentane ring fused to the steroid nucleus. It is a white crystalline solid with a molecular formula of C27H46 and a molecular weight of 374.65 g/mol. 3,5-Cyclocholestane is formed by the cyclization of the side chain of cholesterol, resulting in the formation of a five-membered ring between carbons 3 and 5. 3,5-Cyclocholestane is an important intermediate in the synthesis of various steroidal compounds and has potential applications in the pharmaceutical and chemical industries. It is typically synthesized through various chemical reactions, such as the Diels-Alder reaction or the intramolecular cyclization of cholesterol derivatives. Due to its complex structure and potential applications, 3,5-cyclocholestane remains an interesting subject of study in organic chemistry and related fields.

465-56-5

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465-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 465-56-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 465-56:
(5*4)+(4*6)+(3*5)+(2*5)+(1*6)=75
75 % 10 = 5
So 465-56-5 is a valid CAS Registry Number.

465-56-5Downstream Products

465-56-5Relevant academic research and scientific papers

PHOTOREDUCTION DES ESTERS CARBOXYLIQUES DANS L'HEXAMETHYLPHOSPHORTRIAMIDE (HMPT)

Portella, C.,Deshayes, H.,Pete, J. P.,Scholler, D.

, p. 3635 - 3644 (2007/10/02)

Use of HMPT as solvent in photochemistry allows efficient photoreductions.Alkyl esters and especially non absorbing alkyl acetates are photoreduced in excellent yields into alkanes.In the latter case, a protonating agent is necessary.Numerous examples illustrate the generality and convenience of the reaction.This photoreduction involves an electron transfer from HMPT to ester.

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