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3-aminopregnan-20-one is a steroidal compound derived from the pregnane family, characterized by its unique structure with an amino group at the 3-position and a ketone group at the 20-position. This chemical is known for its potential applications in the pharmaceutical industry, particularly in the development of drugs targeting the central nervous system. It has been studied for its neurosteroid properties, which may influence cognitive functions and mood. The compound's specific role and therapeutic potential are subjects of ongoing research, as it may have implications for treating various neurological disorders.

2135-37-7

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2135-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2135-37-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,3 and 5 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2135-37:
(6*2)+(5*1)+(4*3)+(3*5)+(2*3)+(1*7)=57
57 % 10 = 7
So 2135-37-7 is a valid CAS Registry Number.

2135-37-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(3R,5S,8R,9S,10S,13S,14S,17S)-3-amino-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]ethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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

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More Details:2135-37-7 SDS

2135-37-7Relevant academic research and scientific papers

A novel scalable and stereospecific synthesis of 3α- and 3β-amino-5α-androstan-17-ones and 3α- and 3β-amino- 5α-pregnan-20-ones

Hitchin, James R.,Hamilton, Niall M.,Jordan, Allan M.,Lyons, Amanda J.,Ogilvie, Donald J.

, p. 2868 - 2872 (2012/07/27)

A novel scalable stereoselective synthesis of 3α- and 3β-amino-5α-androstan-17-ones and 3α- and 3β-amino- 5α-pregnan-20-ones has been developed using phthalimide based Mitsunobu chemistry. In all four cases, the products were isolated as single diastereoisomers in high chemical yield and purity without the need for chromatography at any stage in their syntheses.

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