7745-18-8 Usage
Description
(3beta,5alpha,6alpha,10alpha,17beta)-5-bromo-6,19-epoxyandrostane-3,17-diol is a complex chemical compound belonging to the androstane group of steroids. It features a bromine atom and an epoxy group, which contribute to its unique chemical properties and biological activities. (3beta,5alpha,6alpha,10alpha,17beta)-5-bromo-6,19-epoxyandrostane-3,17-diol may hold potential for applications in the pharmaceutical and medical industries, particularly in the development of new drugs for various conditions. Further research is necessary to fully explore its properties and potential uses.
Uses
Used in Pharmaceutical Industry:
(3beta,5alpha,6alpha,10alpha,17beta)-5-bromo-6,19-epoxyandrostane-3,17-diol is used as a chemical compound for the development of new drugs due to its unique chemical properties and biological activities.
Used in Medical Industry:
(3beta,5alpha,6alpha,10alpha,17beta)-5-bromo-6,19-epoxyandrostane-3,17-diol is used as a potential candidate for the development of new treatments for various conditions, given its distinctive structure and characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 7745-18-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,4 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7745-18:
(6*7)+(5*7)+(4*4)+(3*5)+(2*1)+(1*8)=118
118 % 10 = 8
So 7745-18-8 is a valid CAS Registry Number.
7745-18-8Relevant articles and documents
SYNTHESIS OF 19-HYDROXYSTEROIDS I. NEW SYNTHESIS OF 19-HYDROXYTESTOSTERONE
Kovganko, N. V.,Kashkan, Zh. N.,Chernov, Yu. G.
, p. 584 - 588 (2007/10/02)
For obtaining 19-hydroxytestosterone from dehydroepiandrosterone a new scheme of synthesis has been developed the key stages of which are the reduction of the 17-keto group to a 17-alcohol, the functionalization of the 19-methyl group via the bromohydrin with the formation of a 6β,19-epoxide, the selective hydrolysis of the free β-acetoxy group, the conversion of the 3β-hydroxy-5α-bromo derivative into the Δ4-3-ketone, and the reductive cleavage of the 6β,19-epoxide ring.
