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3α-acetoxy-17a-aza-D-homo-5α-androstan-17-one is a complex organic compound belonging to the steroidal alkaloid class. It features a steroidal backbone with a nitrogen atom replacing carbon-17, making it an azasteroid. The molecule has an acetoxy group at the 3α position and a 5α-androstan structure, which is a modified version of the androstane ring system. 3α-acetoxy-17a-aza-D-homo-5α-androstan-17-one is of interest in medicinal chemistry due to its potential biological activities and structural properties that can be explored for drug development. It represents a unique class of compounds that can be further modified and studied for their interactions with various biological targets.

1832-06-0

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1832-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1832-06-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,3 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1832-06:
(6*1)+(5*8)+(4*3)+(3*2)+(2*0)+(1*6)=70
70 % 10 = 0
So 1832-06-0 is a valid CAS Registry Number.

1832-06-0Downstream Products

1832-06-0Relevant academic research and scientific papers

Photo-induced Transformations. Part 44. Formation of Lactams in the Photolysis of Some Steroidal Acetylhydrazones in the Presence of Oxygen

Suginome, Hiroshi,Uchida, Tsutomu

, p. 1356 - 1364 (2007/10/02)

Irradiation of 3α-acetoxy-5α-androstan-17-one acetylhydrazone (3) or 3β-acetoxyandrost-5-en-17-one acetylhydrazone (5) in dioxan in the presence of oxygen afforded 17-oxo-17a-aza-D-homosteroid and its 13α-isomer , while when oxygen was excluded none of these lactams were formed under otherwise similar conditions. 5α-Cholestan-6-one acetylhydrazone (20) under similar conditions also afforded very low yields of 6-aza-D-homo-5α-cholestan-7-one (21) and 7-aza-B-homo-5α-cholestan-6-one (22) upon photolysis.In contrast with the acetylhydrazones, the corresponding hydrazone (2), upon photolysis in dioxan without the exclusion of oxygen, afforded the corresponding azine (13) without any accompanying lactams .There is a distinct difference in behaviour between the hydrazones and the N-acetyl derivatives towards oxygen under irradiation.Although as yet no definite conclusion can be drawn on the mechanism of lactam formation, some plausible paths are discussed.

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