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Tetrahydro-pyran-4-thiol is an organic compound characterized by a six-membered ring structure with four saturated carbon atoms and one sulfur atom. It is a versatile building block in the synthesis of various pharmaceutical products due to its unique chemical properties and reactivity.

203246-71-3

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203246-71-3 Usage

Uses

Used in Pharmaceutical Industry:
Tetrahydro-pyran-4-thiol is used as a building block for the development of various pharmaceutical goods, particularly for the synthesis of MDM2 inhibitors. These inhibitors play a crucial role in the treatment of cancer by targeting the MDM2 protein, which is often overexpressed in various types of cancer cells, leading to the disruption of the p53 tumor suppressor pathway. By inhibiting MDM2, these drugs can potentially restore the function of the p53 protein, thereby promoting apoptosis and inhibiting tumor growth.

Check Digit Verification of cas no

The CAS Registry Mumber 203246-71-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,2,4 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 203246-71:
(8*2)+(7*0)+(6*3)+(5*2)+(4*4)+(3*6)+(2*7)+(1*1)=93
93 % 10 = 3
So 203246-71-3 is a valid CAS Registry Number.
InChI:InChI=1/C5H10OS/c7-5-1-3-6-4-2-5/h5,7H,1-4H2

203246-71-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name oxane-4-thiol

1.2 Other means of identification

Product number -
Other names tetrahydropyran-4-thiol

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:203246-71-3 SDS

203246-71-3Relevant academic research and scientific papers

Nickel-Catalyzed Inter- and Intramolecular Aryl Thioether Metathesis by Reversible Arylation

Delcaillau, Tristan,Bismuto, Alessandro,Lian, Zhong,Morandi, Bill

, p. 2110 - 2114 (2019/12/24)

A nickel-catalyzed aryl thioether metathesis has been developed to access high-value thioethers. 1,2-Bis(dicyclohexylphosphino)ethane (dcype) is essential to promote this highly functional-group-tolerant reaction. Furthermore, synthetically challenging macrocycles could be obtained in good yield in an unusual example of ring-closing metathesis that does not involve alkene bonds. In-depth organometallic studies support a reversible Ni0/NiII pathway to product formation. Overall, this work not only provides a more sustainable alternative to previous catalytic systems based on Pd, but also presents new applications and mechanistic information that are highly relevant to the further development and application of unusual single-bond metathesis reactions.

AMIDO-BENZYL SULFONE AND SULFOXIDE DERIVATIVES

-

Page/Page column 148, (2013/09/12)

The present invention relates to certain amido-benzyl sulfoxide and sulfone compounds, pharmaceutical compositions comprising such compounds, and methods of treatment using such compounds.

PYRIDINYL AND PYRIMIDINYL SULFOXIDE AND SULFONE DERIVATIVES

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Page/Page column 109, (2013/09/12)

Disclosed are certain pyridinyl and pyrimidinyl sulfoxide and sulfone compounds, pharmaceutical compositions comprising such compounds and methods of treatment using such compounds.

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