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38965-27-4

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38965-27-4 Usage

Type

Synthetic androgenic-anabolic steroid

Use

Performance-enhancing drug

Derivative of

Dehydroepiandrosterone (DHEA)

Commonly found in

Dietary supplements and bodybuilding products

Effects

Believed to promote muscle growth and enhance athletic performance

Similar to

Testosterone

Legal status

Banned in many professional sports and classified as a controlled substance in many countries

Potential issues

Potential for abuse and negative health effects

Scientific evidence

Limited evidence supporting its efficacy and safety when used as a performance-enhancing drug.

Check Digit Verification of cas no

The CAS Registry Mumber 38965-27-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,9,6 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 38965-27:
(7*3)+(6*8)+(5*9)+(4*6)+(3*5)+(2*2)+(1*7)=164
164 % 10 = 4
So 38965-27-4 is a valid CAS Registry Number.

38965-27-4SDS

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 [(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] 3,3-dimethylbutanoate

1.2 Other means of identification

Product number -
Other names 17beta-Hydroxyandrost-4-en-3-one 3,3-dimethylbutyrate

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:38965-27-4 SDS

38965-27-4Downstream Products

38965-27-4Relevant articles and documents

Gunatilaka,Sotheeswaran

, p. 980 (1978)

Esterification of Carboxylic Acids with Alcohols Using Benzenesulphonyl and Methanesulphonyl Chlorides

Dharmaratne, H. R. W.,Gunatilaka, A. A. Leslie,Sotheeswaran, S.

, p. 39 - 41 (2007/10/02)

The role of benzene- and methane-sulphonyl chlorides as coupling agents in the esterification of carboxylic acids with alcohols has been investigated.Hindered tertiary alcohols require initial conversion of the acid to the mixed acid-anhydride with benzenesulphonyl chloride.It is necessary to adjust molar ratios for esterification with secondary alcohols so that the intermediate formed is the symmetrical acid anhydride, since mixed acid-anhydrides also give the sulphonates of the alcohols wihich are difficult to separate from the esters.

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