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133586-83-1

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133586-83-1 Usage

Description

(7aS,8aS,8bS,11R,11aR,13aS,13bR)-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 molecule characterized by a cyclopentane ring structure, multiple methyl groups, and a thioether functional group. (7aS,8aS,8bS,11R,11aR,13aS,13bR)-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione features a long hydrocarbon chain and a six-membered cyclic sulfur-containing ring. The presence of the thioether group suggests potential reactivity in biological systems, and the intricate structure indicates a possible role in pharmaceutical or synthetic applications. Further research is necessary to fully comprehend the properties and potential uses of this chemical compound.

Uses

Used in Pharmaceutical Applications:
(7aS,8aS,8bS,11R,11aR,13aS,13bR)-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 pharmaceutical agent for [application reason]. (7aS,8aS,8bS,11R,11aR,13aS,13bR)-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione's complex structure and thioether group may contribute to its reactivity and interaction with biological systems, making it a candidate for further investigation in the development of new drugs.
Used in Synthetic Chemistry:
In the field of synthetic chemistry, (7aS,8aS,8bS,11R,11aR,13aS,13bR)-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 key intermediate or building block for the synthesis of more complex molecules. Its unique structural features, including the cyclopentane ring and thioether group, may facilitate the creation of novel compounds with specific properties and applications.
Used in Chemical Research:
(7aS,8aS,8bS,11R,11aR,13aS,13bR)-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione serves as a subject of study in chemical research, where its properties, reactivity, and potential applications are explored. (7aS,8aS,8bS,11R,11aR,13aS,13bR)-11a,13b-dimethyl-11-[(2R)-6-methylheptan-2-yl]hexadecahydrocyclopenta[1,2]phenanthro[9,8a-d][1,3]oxathiole-6-thione's intricate structure and functional groups make it an interesting target for understanding the behavior of similar molecules and their interactions with biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 133586-83-1 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 133586-83:
(8*1)+(7*3)+(6*3)+(5*5)+(4*8)+(3*6)+(2*8)+(1*3)=141
141 % 10 = 1
So 133586-83-1 is a valid CAS Registry Number.

133586-83-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5α-cholestano [6α,5-d]-1',3'-oxathiolane-2'-thione

1.2 Other means of identification

Product number -
Other names 5alpha-Cholestano(6alpha,5-d)-1',3'-oxathiolane-2'-thione

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:133586-83-1 SDS

133586-83-1Downstream Products

133586-83-1Relevant articles and documents

Synthesis of 1,3-xoathiolane-2-thiones by the reaction of steroidal oxiranes with carbon disulfide

Shamsuzzaman,Salim, Anwar

, p. 5705 - 5708 (1997)

The reaction of 5, 6α-epoxy-5α-cholestane (1), its 3β-acetoxy-(2) and 3β- chloro-(3) analogues with carbon disulfide in THF at room temperature in the presence of Li Br as catalyst afford selectively the corresponding 1,3-oxathiolane-2-thiones (steroidal cyclic cis-dithiocarbonates) (4-6) in high yields.

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