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.
15296-86-3Relevant 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