133586-84-2 Usage
Description
(3S,7aS,8aS,8bS,11R,11aR,13aS,13bR)-3-hydroxy-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione is a complex organic compound with a long and intricate molecular structure. It contains a cyclopentane ring and a thiole (-SH) functional group, as well as several methyl and hydroxyl groups. (3S,7aS,8aS,8bS,11R,11aR,13aS,13bR)-3-hydroxy-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione is a natural product with potential biological activities, and it may be used in pharmaceutical or biological research due to its unique structure and potential therapeutic properties.
Uses
Used in Pharmaceutical Industry:
(3S,7aS,8aS,8bS,11R,11aR,13aS,13bR)-3-hydroxy-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione is used as a potential therapeutic agent for various diseases due to its unique structure and potential biological activities.
Used in Biological Research:
(3S,7aS,8aS,8bS,11R,11aR,13aS,13bR)-3-hydroxy-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione is used as a research tool in biological studies to investigate its potential biological activities and therapeutic properties.
Check Digit Verification of cas no
The CAS Registry Mumber 133586-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,5,8 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 133586-84:
(8*1)+(7*3)+(6*3)+(5*5)+(4*8)+(3*6)+(2*8)+(1*4)=142
142 % 10 = 2
So 133586-84-2 is a valid CAS Registry Number.
133586-84-2Relevant articles and documents
SYNTHESIS OF STEROIDAL OXATHIOLANE THIONES
Shafiullah,Shamsuzzaman,Pathak, Rajesh Kumar
, p. 701 - 704 (2007/10/02)
The reaction of 5,6α-oxido-5α-cholestane (1) with carbon disulfide in the presence of triethylamine at room temperature affords 5α-cholestano-1',3'-oxathiolane-2'-thione (5).Under similar reaction conditions, its 3β-hydroxy (2), 3β-acetoxy (3) and 3β-chloro (4) analogues give 3β-hydroxy-5α-cholestano-1',3'-oxathiolane-2'-thione (6), 3β-acetoxy-5α-cholestano-1',3'-oxathiolane-2'-thione (7), and 3β-chloro-5α-cholestano-1',3'-oxathiolane-2'-thione (8), respectively.The structures of these compounds have been established on t he basis of elemental analyses and the spectral values.
