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601-03-6

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601-03-6 Usage

General Description

The chemical compound "3beta,17,21-trihydroxy-5beta-pregnan-20-one" is a steroid hormone and a metabolite of the hormone progesterone. It is also known as 20-dihydroprogesterone and is produced in the body as part of the normal metabolism of progesterone. 3beta,17,21-trihydroxy-5beta-pregnan-20-one has been found to have neuroprotective and anti-inflammatory properties, and it has been suggested to play a role in the regulation of the central nervous system. It is also being studied for its potential therapeutic applications in conditions such as traumatic brain injury, multiple sclerosis, and other neurological disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 601-03-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,0 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 601-03:
(5*6)+(4*0)+(3*1)+(2*0)+(1*3)=36
36 % 10 = 6
So 601-03-6 is a valid CAS Registry Number.

601-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3β,5α-Tetrahydro Reichstein's Substance S

1.2 Other means of identification

Product number -
Other names 3BETA,17,21-TRIHYDROXY-5BETA-PREGNAN-20-ONE

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:601-03-6 SDS

601-03-6Relevant articles and documents

A convenient synthesis of the side chain of loteprednol etabonate - An ocular soft corticosteroid from 20-oxopregnanes using metal-mediated halogenation as a key reaction

Chowdhury, Pritish,Borah, Juri Moni,Goswami, Papori,Das, Archana Moni

experimental part, p. 497 - 501 (2011/05/09)

A facile synthesis of the side chain of loteprednol etabonate, namely, chloromethyl-17α-[(ethoxycarbonyl))oxy]-11β-hydro of loteprednol etabonate, viz., chloromethyl-17α-[(ethoxycarbonyl))oxy]-11xy-3- oxoandrosta-1,4-diene-17β-carboxylate - an ocular soft corticosteroid, has been described starting from a 20-oxopregnane, namely, 3β-acetoxy-pregn- 5(6),16(17)-diene-20-one (16-dehydropregnenolone acetate, i.e., 16-DPA) using our recently developed metal-mediated halogenation as a key reaction.

IDENTIFICATION IN HUMAN URINE OF THE 21-GLUCURONATE OF

PASQUALINI,JAYLE

, p. 2345 - 2347 (2007/10/14)

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