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N-[(20S)-3α-Dimethylamino-5α-pregnan-20-yl]-N-methylacetamide is a complex organic compound derived from the leaves of Sarcococca pruniformis, a plant that yields four closely related alkaloids. N-[(20S)-3α-Dimethylamino-5α-pregnan-20-yl]-N-methylacetamide forms colorless needles when crystallized from Me2CO (dimethyl carbonate). Upon hydrolysis with 1N H2SO4 (sulfuric acid), it produces the deacetyl compound, C22H44N2, with a melting point of 94-96°C.

15437-92-0

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15437-92-0 Usage

Uses

1. Used in Pharmaceutical Industry:
N-[(20S)-3α-Dimethylamino-5α-pregnan-20-yl]-N-methylacetamide is used as a pharmaceutical compound for its potential therapeutic applications. The compound's unique structure and properties make it a promising candidate for the development of new drugs targeting various health conditions.
2. Used in Research and Development:
In the field of research and development, N-[(20S)-3α-Dimethylamino-5α-pregnan-20-yl]-N-methylacetamide serves as a valuable compound for studying its chemical properties, interactions with other molecules, and potential applications in drug discovery. Its unique structure allows researchers to explore its potential in various biological and medicinal contexts.
3. Used in Chemical Synthesis:
N-[(20S)-3α-Dimethylamino-5α-pregnan-20-yl]-N-methylacetamide can be utilized as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique functional groups and structural features make it a versatile building block for the development of novel molecules with specific properties and applications.
4. Used in Analytical Chemistry:
N-[(20S)-3α-Dimethylamino-5α-pregnan-20-yl]-N-methylacetamide can also be employed in analytical chemistry for the development of new methods and techniques for the identification, quantification, and characterization of similar compounds. Its unique properties can be exploited to improve the sensitivity, selectivity, and accuracy of analytical methods, leading to better understanding and control of complex chemical systems.

References

Chatterjee et al., Tetrahedron Lett., 67 (1965)

Check Digit Verification of cas no

The CAS Registry Mumber 15437-92-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,3 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15437-92:
(7*1)+(6*5)+(5*4)+(4*3)+(3*7)+(2*9)+(1*2)=110
110 % 10 = 0
So 15437-92-0 is a valid CAS Registry Number.

15437-92-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names Acetamide,N-[(3a,5a,20S)-3-(dimethylamino)pregnan-20-yl]-N-methyl-(9CI)

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:15437-92-0 SDS

15437-92-0Upstream product

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