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65065-57-8

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65065-57-8 Usage

General Description

(3beta,5alpha)-16-formylandrost-16-en-3-yl acetate is a chemical compound with a complex molecular structure. It belongs to the class of androstanes, which are steroids derived from androstane. (3beta,5alpha)-16-formylandrost-16-en-3-yl acetate is an acetate ester, meaning it contains the ester functional group formed from acetic acid. The presence of a formyl group at the 16th position and an acetate group indicates that it is a derivative of androst-16-en-3-yl acetate. This chemical has potential applications in the pharmaceutical industry, particularly in the synthesis of steroid hormones and other bioactive compounds. However, further research and analysis are required to fully understand its properties and potential uses.

Check Digit Verification of cas no

The CAS Registry Mumber 65065-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,0,6 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 65065-57:
(7*6)+(6*5)+(5*0)+(4*6)+(3*5)+(2*5)+(1*7)=128
128 % 10 = 8
So 65065-57-8 is a valid CAS Registry Number.

65065-57-8SDS

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 2-(5,7-dihydrobenzo[d][2]benzazepin-6-yl)ethanol

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:65065-57-8 SDS

65065-57-8Downstream Products

65065-57-8Relevant articles and documents

Steroids, XLV. Neighbouring Group Participation, XII. Decomposition of (Z)-16-Amidomethylene-17β-hydroxysteroids Mediated by Neighbouring Group Participation

Vincze, Iren,Somlai, Csaba,Schneider, Gyula,Dombi, Gyoergy,Mak, Marianna

, p. 187 - 192 (2007/10/02)

The sodium tetrahydroborate reduction of 16-methylene>-17-ketosteroids 1aa, 2aa and 2ba affords (Z)-16- and (E)-16-methylene>-17β-hydroxysteroids (Z)-3, (E)-3, (Z)-4b, (Z)-4a, (Z)-5c and (E)-5a.The N-acetyl group

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