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3β-Acetyloxy-17-hydroxy-5α-pregnan-20-one is a chemical compound that belongs to the class of pregnane steroids. It is a derivative of progesterone, a hormone that is involved in the regulation of the menstrual cycle and pregnancy. 3β-Acetyloxy-17-hydroxy-5α-pregnan-20-one contains an acetyloxy group at the C3 position and a hydroxy group at the C17 position of the pregnane structure. Additionally, it features a ketone group at the C20 position and a double bond at the C5 position. Its unique structure endows it with potential applications in various fields, particularly in pharmaceuticals and scientific research.

5456-44-0

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5456-44-0 Usage

Uses

Used in Pharmaceutical Industry:
3β-Acetyloxy-17-hydroxy-5α-pregnan-20-one is used as a progestin-based medication for the development of contraceptives and hormone replacement therapies. Its structure allows it to mimic the effects of progesterone, providing a foundation for creating medications that can help regulate hormonal balance and prevent pregnancy.
Used in Scientific Research:
In the field of scientific research, 3β-Acetyloxy-17-hydroxy-5α-pregnan-20-one serves as a valuable tool for studying hormone metabolism and signaling pathways. Its derivative nature from progesterone makes it instrumental in understanding the complex interactions and effects of hormones within the body, which can contribute to advancements in endocrinology and reproductive health.

Check Digit Verification of cas no

The CAS Registry Mumber 5456-44-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,5 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5456-44:
(6*5)+(5*4)+(4*5)+(3*6)+(2*4)+(1*4)=100
100 % 10 = 0
So 5456-44-0 is a valid CAS Registry Number.
InChI:InChI=1/C23H36O4/c1-14(24)23(26)12-9-20-18-6-5-16-13-17(27-15(2)25)7-10-21(16,3)19(18)8-11-22(20,23)4/h16-20,26H,5-13H2,1-4H3/t16-,17-,18+,19-,20-,21-,22-,23-/m0/s1

5456-44-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3S,5S,8R,9S,10S,13S,14S,17R)-17-acetyl-17-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-3-yl] acetate

1.2 Other means of identification

Product number -
Other names 5|A-pregnan-20-one,3|A,17-dihydroxy-,3-acetate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5456-44-0 SDS

5456-44-0Relevant academic research and scientific papers

REARRANGEMENT SPINAL DU DIMETHYL-4,4 EPOXY-6α,20α(5α)ANDROSTANE AVEC LE TRICHLORURE DE BORE

Fetizon, Marcel,Sozzi, Georges

, p. 61 - 68 (2007/10/02)

A backbone rearrangement of 4,4 dimethyl 6α,20α epoxy (5α)androstane with BCl3 is described.The structures of the resulting compounds have been elucidated either by synthesis from 3β-acetoxy (5α)pregnane 20-one, or by X rays diffraction.

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