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2862-58-0

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2862-58-0 Usage

General Description

"(3beta)-pregn-5-en-3-ol" is a chemical compound that belongs to the class of pregnanes, which are a group of steroid hormones. Its molecular structure consists of a 5-membered ring, with a hydroxyl group attached to the third carbon of the steroid backbone. (3beta)-pregn-5-en-3-ol is a precursor to the synthesis of various hormones such as progesterone, estrogen, and testosterone. It plays a crucial role in the regulation of the reproductive system and other physiological processes in the body. Additionally, "(3beta)-pregn-5-en-3-ol" is also used in the production of pharmaceuticals and research purposes to study hormone regulation and related medical conditions.

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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