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3,17β-Diacetoxy-10α-androsta-3,5-dien is a steroidal compound characterized by the presence of two acetoxy groups at the 3 and 17β positions, and a double bond between carbons 3 and 5. This molecule is a derivative of androstane, a naturally occurring steroid hormone, and features a 10α-configuration, which means the hydroxyl group at the 10 position is oriented in the alpha position. The compound is known for its potential applications in the synthesis of various pharmaceuticals and has been studied for its biological activities, although its specific uses and effects can vary. It is important to note that the handling and application of such compounds are subject to regulatory controls due to their potential impact on human health and the environment.

3591-21-7

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3591-21-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3591-21-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,9 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3591-21:
(6*3)+(5*5)+(4*9)+(3*1)+(2*2)+(1*1)=87
87 % 10 = 7
So 3591-21-7 is a valid CAS Registry Number.

3591-21-7Upstream product

3591-21-7Relevant academic research and scientific papers

Stereoscopic synthesis of 4β-deutero-Δ5-3-ketosteroids

Segal,Fradkina,Torgov

, p. 213 - 216 (1969)

Simple methods for the stereospecific synthesis of 4β-deutero-Δ5-3-ketosteroids have been developed involving the reduction of 3-acetoxy-Δ3, 5-steroids with lithium aluminum hydride and subsequent decomposition with deuterium oxide a

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