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3β-acetoxy-5α-androstan-17-one is a steroidal ketone derivative, specifically a 5α-reduced androstane with an acetoxy group at the 3β position and a ketone group at the 17 position. 3β-acetoxy-5α-androstan-17-one is a synthetic analog of natural androgens, which are male sex hormones, and is structurally similar to testosterone. It is used in various pharmaceutical applications, including the treatment of hormonal imbalances and certain medical conditions. The acetoxy group at the 3β position increases the compound's lipophilicity, which can enhance its absorption and bioavailability. The 5α-reduced structure also plays a role in its biological activity, as it affects the compound's interaction with androgen receptors. Overall, 3β-acetoxy-5α-androstan-17-one is a significant compound in the field of endocrinology and pharmaceuticals due to its potential therapeutic applications.

1098-12-0

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1098-12-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1098-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,9 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1098-12:
(6*1)+(5*0)+(4*9)+(3*8)+(2*1)+(1*2)=70
70 % 10 = 0
So 1098-12-0 is a valid CAS Registry Number.

1098-12-0Relevant academic research and scientific papers

A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of α,β-unsaturated ketoximes

Yan, Zhaohua,Xu, Yun,Tian, Weisheng

supporting information, p. 7186 - 7189 (2015/02/02)

The reaction of α,β-unsaturated ketoximes with fluoroalkanosulfonyl fluorides in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) underwent the Beckmann rearrangement smoothly to afford the corresponding acid-sensitive enamides in moderate to excellent yields, which provides a new efficient method for the preparation of acid-sensitive enamides.

STEROIDS .LIII. TRANSFORMATION OF 3β-ACETOXY-5α-ANDROSTAN-17-ONE INTO 17α- AND 17β-AMINO DERIVATIVES OF 5α-ANDROSTAN-3β-OL

Nadaraia, N. Sh.,Sladkov, V. I.,Kuleshova, L. N.,Suvorov, N. N.

, p. 481 - 485 (2007/10/02)

The epimeric 17α- and 17β-amino-5α-androstan-3β-ols were synthesized from 3β-acetoxy-5α-androstan-17-one.The configurations at the C17 atom were demonstrated by the 1H NMR method.

Process for the preparation of 17β-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone

-

, (2008/06/13)

A new process utilizing certain novel intermediates for the preparation of 17β-hydroxy-3-oxo-17α-pregn-4-ene-21-carboxylic acid γ-lactone is described herein. The procedure utilizes readily available and inexpensive sarsasaponin as starting material.

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