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15296-86-3

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15296-86-3 Usage

General Description

{[(phenylsulfanyl)methyl]sulfonyl}benzene is a chemical compound with a molecular formula C14H14S2O2. It is a benzene derivative with two sulfur atoms and a single methyl group attached to the benzene ring. The compound is a sulfide, featuring both a sulfonyl and a phenylsulfanyl group. It is commonly used as a starting material in organic synthesis to create various sulfur-containing compounds. Additionally, it has been studied for its potential applications in pharmaceuticals and agrochemicals due to its unique structural properties. The compound's diverse functionality makes it an important building block in the production of a wide range of chemical compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 15296-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,2,9 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15296-86:
(7*1)+(6*5)+(5*2)+(4*9)+(3*6)+(2*8)+(1*6)=123
123 % 10 = 3
So 15296-86-3 is a valid CAS Registry Number.

15296-86-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(phenylsulfanyl)methyl phenyl sulfone

1.2 Other means of identification

Product number -
Other names Phenylmercaptomethyl-phenyl-sulfon

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:15296-86-3 SDS

15296-86-3Relevant articles and documents

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Bordwell,F.G.,Jarvis,B.B.

, p. 1182 - 1185 (1968)

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Preparation of 2-Halogeno S-Phenyl Thioesters from 2-Phenylsulphonyl-2-phenylthiooxiranes. Crystal Structures of 2-Phenylsulphonyloxiranes

Hewkin, Cheryl T.,Jackson, Richard F. W.,Clegg, William

, p. 3091 - 3102 (2007/10/02)

1-Phenylsulphonyl-1-phenylthioalkenes 8 are prepared with high stereoselectivity as (E) isomers in a one-pot process by reaction of phenyl phenylthiomethyl sulphone 9 with aldehydes, followed by elimination.Nucleophilic epoxidation of these alkenes with l

Asymmetric Microbial Oxidation of Formaldehyde Dithioacetals

Okamoto, Yasushi,Ohta, Hiromichi,Tsuchihashi, Gen-ichi

, p. 2049 - 2052 (2007/10/02)

Incubation of formaldehyde dithioacetals with growing cells of Corynebacterium equi IFO 3730 afforded a variety of oxidation products depending on the structure of the substrate.The products with sulfoxide moiety were optically pure and had R configuratio

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