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N-(3-oxoandrost-4-en-17-yl)acetamide, also known as 17-acetoxy-3-oxo-4-androstenamide, is a synthetic steroidal compound derived from the androstane family. It features a 3-oxo group, which is a carbonyl functional group at the 3-position, and a 17-acetoxy group, which is an acetate ester at the 17-position. This chemical structure is characterized by a four-ring steroid nucleus with a double bond between carbons 4 and 5, and a ketone group at the 3-position. The acetamide group is attached to the nitrogen atom, which is part of the steroid's A-ring. N-(3-oxoandrost-4-en-17-yl)acetamide is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a research tool for studying steroidal compounds. However, it is important to note that the specific biological activity, pharmacological properties, and safety profile of N-(3-oxoandrost-4-en-17-yl)acetamide have not been fully established and would require further investigation.

1865-62-9

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1865-62-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1865-62-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1865-62:
(6*1)+(5*8)+(4*6)+(3*5)+(2*6)+(1*2)=99
99 % 10 = 9
So 1865-62-9 is a valid CAS Registry Number.

1865-62-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 2-Methyl-17|A-estradiol

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

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More Details:1865-62-9 SDS

1865-62-9Relevant academic research and scientific papers

A FACILE SYNTHESIS OF STEROIDAL Δ4-3-KETONES USING PYRIDINIUM CHLOROCHROMATE (PCC)

Parish, Edward J.,Honda, Hiroshi

, p. 1167 - 1174 (2007/10/02)

Pyridinium chlorochromate (PCC), in refluxing benzene, has been found to be an affective and convenient reagent for the oxidation and concomitant isomerization of steroidal Δ5-3β-alcohols to the corresponding Δ4-3-ketones in high yield.

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