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2862-58-0

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2862-58-0 Usage

Description

(3beta)-pregn-5-en-3-ol, a member of the pregnane class of steroid hormones, features a molecular structure with a 5-membered ring and a hydroxyl group attached to the third carbon of the steroid backbone. (3beta)-pregn-5-en-3-ol serves as a precursor for the synthesis of essential hormones such as progesterone, estrogen, and testosterone, playing a vital role in the regulation of the reproductive system and other physiological processes.

Uses

Used in Pharmaceutical Industry:
(3beta)-pregn-5-en-3-ol is used as a key intermediate in the synthesis of various hormones for pharmaceutical applications, including progesterone, estrogen, and testosterone. These hormones are crucial for the treatment of hormonal imbalances and related conditions.
Used in Research and Development:
(3beta)-pregn-5-en-3-ol is utilized as a research compound to study hormone regulation and investigate related medical conditions. This helps in advancing our understanding of the endocrine system and contributes to the development of new therapeutic approaches for hormone-related disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 2862-58-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,6 and 2 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2862-58:
(6*2)+(5*8)+(4*6)+(3*2)+(2*5)+(1*8)=100
100 % 10 = 0
So 2862-58-0 is a valid CAS Registry Number.

2862-58-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,8S,9S,10R,13R,14S,17S)-17-ethyl-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

1.2 Other means of identification

Product number -
Other names 5-pregnen-3|A-ol

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:2862-58-0 SDS

2862-58-0Relevant articles and documents

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Jeanloz

, p. 2281 (1950)

-

METHODS OF ACTIVATING MICROGLIAL CELLS

-

Page/Page column 51; 58, (2020/02/23)

The present disclosure provides methods of using compositions that inhibit SH2-containing inositol 5'-phosphatases (SHIPs) for activating microglial cells, as well as methods for using such compositions for treatment or ameliorating of neurodegenerative disorders in a subject.

Synthesis of Triaromatic Steroid Hydrocarbons Methylated at Position 2, 3 or 6: Molecular Fossils of Yet Unknown Biological Origin.

Lichtfouse, Eric,Albrecht, Pierre

, p. 1731 - 1744 (2007/10/02)

C21-29 triaromatic steroid hydrocarbons bearing a methyl group at unusual positions 2, 3 or 6 have been synthesized from pregnenolone, cholesterol or stigmasterol via stera-3,5-dienes.Their occurence in various sedimentary rocks and petroleums suggests the presence of yet unknown biological precursors.

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