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3β-hydroxyl-5-pregnen-20-one acetate, also known as 3β-acetoxy-5-pregnen-20-one, is a steroidal compound derived from the pregnane family. It is characterized by the presence of a hydroxyl group at the 3β position and an acetate group at the 20 position. This chemical is a synthetic derivative of the naturally occurring steroid hormone pregnenolone, which plays a crucial role in the synthesis of other steroid hormones such as cortisol, aldosterone, and various sex hormones. The acetate group in 3β-hydroxyl-5-pregnen-20-one acetate increases its lipophilicity, potentially affecting its pharmacokinetics and bioavailability. 3β-hydroxyl-5-pregnen-20-one acetate is of interest in medical research due to its potential applications in the treatment of various hormonal imbalances and conditions related to steroid hormone deficiencies or disorders.

5223-98-3

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5223-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5223-98-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,2 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5223-98:
(6*5)+(5*2)+(4*2)+(3*3)+(2*9)+(1*8)=83
83 % 10 = 3
So 5223-98-3 is a valid CAS Registry Number.

5223-98-3Relevant academic research and scientific papers

A simple procedure for selective reduction of α,β-unsaturated carbonyl compounds using Al-NiCl2 system

Hazarika,Barua

, p. 6567 - 6570 (1989)

A combination of aluminium and nickel chloride in THF has been shown to effect the selective reduction of the olefinic double bond of the α-enone system. Isolated double bonds and aliphatic carbonyls remain unaffected under these conditions. However, aromatic aldehydes and ketones are converted to the corresponding hydroxy compounds by this system in good yields.

Modified steroids 103. Splitting of the 17-C-N bond of 16,17α-epimino-20-ketgsteroids and their 20-hydrazones by reaction with thioacetic acid

Kamernitskii,Turupa,Fadeeva,Pavlov

, p. 825 - 831 (2007/10/10)

1. The reactions of 16,17 α-eplminopregn-5-en-3 β-ol-20-one and its 20-carbethoxyhydrazone with thioacetic acid proceed with different stereochemical direction of scission of the aziridine ring at the tertiary 17-C atom. Schemes to explain the differences are proposed. 2. A new class of heterocyclic compounds, 2′-methyl-[16,17α-d]-thiazoline 20-ketosteroids, has been obtained.

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