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3α-Hydroxyandrosten-(5), also known as 3α-hydroxy-5-androsten-17-one, is a steroidal compound derived from the androstane family. It is characterized by the presence of a hydroxyl group at the 3α position and a double bond at the 5 position. This chemical is an important intermediate in the synthesis of various steroidal hormones and pharmaceuticals, such as testosterone and other anabolic steroids. The compound plays a crucial role in the biosynthesis of sex hormones and has potential applications in the development of drugs for treating hormonal imbalances and related conditions.

5232-33-7

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5232-33-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5232-33-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,3 and 2 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5232-33:
(6*5)+(5*2)+(4*3)+(3*2)+(2*3)+(1*3)=67
67 % 10 = 7
So 5232-33-7 is a valid CAS Registry Number.

5232-33-7Downstream Products

5232-33-7Relevant academic research and scientific papers

A Mild Method for the Conversion of 1,3-Glycols into Unsaturated Alcohols

Ackland, Mark J.,Gordon, John F.,Hanson, James R.,Yeoh, Boon Leng,Ratcliffe, Arnold H.

, p. 2013 - 2018 (2007/10/02)

Some transformations of 1,3-glycols utilizing dimethylformamide dimethyl acetal have been examined with the diterpenoids aphidicolin and foliol and some steroids as substrates.Axial alcohols with a suitably disposed trans hydrogen atom undergo an elimination reaction to give the formate of an unsaturated alcohol via the quaternary salt of the cyclic formamido acetal.

A Mild Method for the Preparation of Unsaturated Alcohols from 1,3-Glycols via Dimethylformamide Acetals

Ackland, Mark J.,Gordon, John F.,Hanson, James R.,Yeoh, Boon Leng,Ratcliffe, Arnold H.

, p. 1756 - 1757 (2007/10/02)

Provided it possesses a hydrogen atom suitably placed for elimination, a 1,3-glycol may be converted into an unsaturated alcohol via quaternization of its dimethylformamide acetal.

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