15296-86-3 Usage
Description
[(phenylsulfanyl)methyl]sulfonylbenzene, with the molecular formula C14H14S2O2, is a benzene derivative characterized by the presence of two sulfur atoms and a single methyl group attached to the benzene ring. [(phenylsulfanyl)methyl]sulfonylbenzene, classified as a sulfide, features both a sulfonyl and a phenylsulfanyl group, endowing it with unique structural properties that make it a versatile building block in the synthesis of various sulfur-containing compounds.
Uses
Used in Organic Synthesis:
[(phenylsulfanyl)methyl]sulfonylbenzene is used as a starting material in organic synthesis for the creation of a wide range of sulfur-containing compounds. Its diverse functionality allows for the development of various chemical products.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, [(phenylsulfanyl)methyl]sulfonylbenzene is used as a key intermediate in the synthesis of potential drug candidates. Its unique structural properties make it a valuable component in the development of new medications.
Used in Agrochemical Applications:
Similarly, in the agrochemical industry, [(phenylsulfanyl)methyl]sulfonylbenzene is utilized as a starting material for the synthesis of compounds with potential applications in agriculture, such as pesticides and other chemical products designed to enhance crop protection and yield.
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
-
Bordwell,F.G.,Jarvis,B.B.
, p. 1182 - 1185 (1968)
-
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
