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testosterone pivalate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21549-54-2

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21549-54-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21549-54-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,4 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 21549-54:
(7*2)+(6*1)+(5*5)+(4*4)+(3*9)+(2*5)+(1*4)=102
102 % 10 = 2
So 21549-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C24H36O3/c1-22(2,3)21(26)27-20-9-8-18-17-7-6-15-14-16(25)10-12-23(15,4)19(17)11-13-24(18,20)5/h14,17-20H,6-13H2,1-5H3/t17-,18-,19-,20-,23-,24-/m0/s1

21549-54-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-oxoandrost-4-ene-17β-yl pivalate

1.2 Other means of identification

Product number -
Other names 17β-pivaloyloxyandrost-4-en-3-one

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:21549-54-2 SDS

21549-54-2Relevant academic research and scientific papers

The microbiological hydroxylation of 4β-hydroxy-4α-methyl-5α androstanes by Cephalosporium aphidicola

Bensasson, Caroline S.,Chevolot, Yvan,Hanson, James R.,Quinton, Jacques

, p. 25 - 30 (1999)

Some 4β-hydroxy-4α-methyl-5α-androstanes were synthesized and their microbiological hydroxylation by Cephalosporium aphidicola was examined in order to explore the possibility of a biosynthetically patterned methylcarbinol: vicinal glycol biotransformation; however the substrates were hydroxylated mainly at C-7.

GLUCOSYLATION OF SOME STEROIDAL 17-HYDROXY DERIVATIVES

Cerny, Ivan,Pouzar, Vladimir,Drasar, Pavel,Havel, Miroslav

, p. 362 - 374 (2007/10/02)

Eight 17-monoglucosides derived from androst-5-ene-3,17-diol, 14β-androst-5-ene-3,17-diol, 5β-androstane-3,17-diol and estradiol derivatives differing in configuration in the positions 17 and 3, have been prepared.The silver silicate - catalyzed glycosyla

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