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4H-Thiopyran-4-one, 2-phenyl-6-[(phenylmethyl)thio]- is a complex organic chemical compound with the molecular formula C17H14OS2. It is a derivative of 4H-thiopyran-4-one, featuring a phenyl group at the 2nd position and a phenylmethylthio group at the 6th position. 4H-Thiopyran-4-one, 2-phenyl-6-[(phenylmethyl)thio]- is characterized by its unique structure, which includes a thiopyran ring, a phenyl ring, and a phenylmethylthio group. It is an important intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its versatile chemical properties and potential reactivity. The compound's structure and properties make it a valuable building block in the development of new molecules with specific biological activities.

113544-17-5

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113544-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113544-17-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,5,4 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 113544-17:
(8*1)+(7*1)+(6*3)+(5*5)+(4*4)+(3*4)+(2*1)+(1*7)=95
95 % 10 = 5
So 113544-17-5 is a valid CAS Registry Number.

113544-17-5SDS

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 2-benzylsulfanyl-6-phenylthiopyran-4-one

1.2 Other means of identification

Product number -
Other names 4H-Thiopyran-4-one,2-phenyl-6-[(phenylmethyl)thio]

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

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More Details:113544-17-5 SDS

113544-17-5Downstream Products

113544-17-5Relevant academic research and scientific papers

INTRAMOLECULAR MICHAEL AND ANTI-MICHAEL ADDITIONS OF THIOLATE TO CONJUGATED ACETYLENIC KETONES

Rudorf, Wolf-Dieter,Schwarz, Ralf

, p. 4267 - 4270 (2007/10/02)

The reaction of acetylenic ketones 1 with carbon disulfide in the basic system sodium hydride/dimethylformamide and subsequent intramolecular cyclization to 4H-thiopyran-4-ones 3 and 3(2H)-thiophenones 4 are reported.

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