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N-[(20S)-4β-Acetoxy-20-(dimethylamino)-5α-pregnan-3α-yl]-N-methylbenzamide is a pregnane alkaloid derivative that is optically active and has been identified in Pachysandra terminalis Sieb. et Zucco. Its structure has been confirmed through spectroscopic evidence and chemical analysis, featuring a 4β-acetoxy-3α-benzoylmethylamino-20α-dimethylamino-5α-pregnan configuration.

6879-28-3

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6879-28-3 Usage

Uses

Used in Pharmaceutical Industry:
N-[(20S)-4β-Acetoxy-20-(dimethylamino)-5α-pregnan-3α-yl]-N-methylbenzamide is used as a pharmaceutical compound for its potential therapeutic applications. N-[(20S)-4β-Acetoxy-20-(dimethylamino)-5α-pregnan-3α-yl]-N-methylbenzamide's unique structure and optical activity suggest that it may have specific interactions with biological targets, making it a candidate for the development of new drugs or therapies.
Used in Research and Development:
In the field of chemical research and development, N-[(20S)-4β-Acetoxy-20-(dimethylamino)-5α-pregnan-3α-yl]-N-methylbenzamide can be utilized as a starting material or a reference compound for the synthesis of novel steroidal compounds. Its unique structure may provide insights into the design and synthesis of new molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Used in Analytical Chemistry:
N-[(20S)-4β-Acetoxy-20-(dimethylamino)-5α-pregnan-3α-yl]-N-methylbenzamide can also be employed in analytical chemistry as a reference standard or a calibration standard for the development and validation of analytical methods, such as high-performance liquid chromatography (HPLC), mass spectrometry (MS), or nuclear magnetic resonance (NMR) spectroscopy. Its optical activity and unique structure make it a valuable tool for the accurate determination of other related compounds in complex mixtures.

References

Tomita, Uyeo, Kikuchi., Tetrahedron Lett., 1053 (1964) Synthesis: Kikuchi, Nishinaga, Yoshimura., Chern. Pharrn. Bull. (Tokyo), 19, 1886 (1971)

Check Digit Verification of cas no

The CAS Registry Mumber 6879-28-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6879-28:
(6*6)+(5*8)+(4*7)+(3*9)+(2*2)+(1*8)=143
143 % 10 = 3
So 6879-28-3 is a valid CAS Registry Number.
InChI:InChI=1/C33H50N2O3/c1-21(34(5)6)25-15-16-26-24-13-14-28-30(38-22(2)36)29(35(7)31(37)23-11-9-8-10-12-23)18-20-33(28,4)27(24)17-19-32(25,26)3/h8-12,21,24-30H,13-20H2,1-7H3/t21?,24?,25-,26?,27?,28+,29?,30-,32-,33-/m1/s1

6879-28-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names Pachysandrine A

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:6879-28-3 SDS

6879-28-3Upstream product

6879-28-3Downstream Products

6879-28-3Relevant academic research and scientific papers

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