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71658-22-5

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71658-22-5 Usage

Type

Synthetic steroid hormone

Class

Corticosteroid

Use

Anti-inflammatory and immunosuppressive agent

Effects

Potent effects on the body's immune response

Conditions treated

Inflammatory disorders such as asthma, arthritis, and allergic reactions

Mechanism of action

Inhibits the production of inflammatory substances in the body

Additional use

Replacement therapy for natural corticosteroids in cases of adrenal insufficiency

Importance

Crucial role in the management of various health conditions and in medical treatments

Check Digit Verification of cas no

The CAS Registry Mumber 71658-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,5 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71658-22:
(7*7)+(6*1)+(5*6)+(4*5)+(3*8)+(2*2)+(1*2)=135
135 % 10 = 5
So 71658-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C22H32O2/c1-14(13-23)18-6-7-19-17-5-4-15-12-16(24)8-10-21(15,2)20(17)9-11-22(18,19)3/h8,10,12,14,17-20,23H,4-7,9,11,13H2,1-3H3/t14?,17-,18+,19-,20-,21-,22+/m0/s1

71658-22-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (8S,9S,10R,13S,14S,17R)-17-(1-hydroxypropan-2-yl)-10,13-dimethyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

1.2 Other means of identification

Product number -
Other names EINECS 275-773-2

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:71658-22-5 SDS

71658-22-5Upstream product

71658-22-5Downstream Products

71658-22-5Relevant articles and documents

ISOLATION AND THE STRUCTURE OF THE PRODUCTS OF CHOLESTEROL BIODEGRADATION BY THE MUTANT Mycobacterium sp. CCM 3529

Mickova, Ruzena,Hutlova, Hana,Pihera, Pavel,Protiva, Jiri,Schwarz, Vladimir

, p. 1110 - 1113 (2007/10/02)

During the biodegradation of cholesterol by the mutant Mycobacterium sp.CCM 3529 1,4-androstadiene-3,17-dione (II) is formed as the main product.The following compounds were identified as characteristic by-products: a mixture of methyl esters IV and V in a 1:3 ratio, 4-androstene-3,17-dione (III), 22-hydroxy derivative I, 17β-hydroxy-4-androsten-3-one (XIII) and 17β-hydroxy-1,4-androstadien-3-one (XII).

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