16873-35-1 Usage
Description
(3-(phenylsulfanyl)-2,2-bis[(phenylsulfanyl)methyl]propylsulfanyl)benzene is a complex organic compound belonging to the thioether class, characterized by the presence of multiple sulfur-sulfur and sulfur-carbon bonds within its molecular structure. (3-(phenylsulfanyl)-2,2-bis[(phenylsulfanyl)methyl]propylsulfanyl)benzene features multiple benzene rings and sulfur atoms, endowing it with unique chemical and physical properties.
Uses
Used in Organic Synthesis:
(3-(phenylsulfanyl)-2,2-bis[(phenylsulfanyl)methyl]propylsulfanyl)benzene is used as a building block in organic synthesis for creating a variety of complex organic molecules. Its unique structure allows for versatile chemical reactions and the formation of new compounds with potential applications in various fields.
Used in Materials Science:
In the field of materials science, (3-(phenylsulfanyl)-2,2-bis[(phenylsulfanyl)methyl]propylsulfanyl)benzene may be utilized for the development of novel materials with specific properties. Its sulfur-containing structure could contribute to the creation of materials with enhanced thermal stability, electrical conductivity, or other desirable characteristics.
Used in Pharmaceutical Research:
(3-(phenylsulfanyl)-2,2-bis[(phenylsulfanyl)methyl]propylsulfanyl)benzene holds potential in pharmaceutical research as a precursor for the synthesis of new drug candidates. Its complex structure and reactivity may lead to the discovery of compounds with therapeutic properties, contributing to the development of innovative medications.
Check Digit Verification of cas no
The CAS Registry Mumber 16873-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,8,7 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 16873-35:
(7*1)+(6*6)+(5*8)+(4*7)+(3*3)+(2*3)+(1*5)=131
131 % 10 = 1
So 16873-35-1 is a valid CAS Registry Number.
16873-35-1Relevant articles and documents
Tetrakis-sulphoxides: a New Type of Phase-transfer Catalyst for Nocleophilic Displacements and Alkylations
Fujihara, Hisashi,Imaoka, Koji,Furukawa, Naomichi,Oae, Shigeru
, p. 333 - 336 (2007/10/02)
Tetrakis(alkylsulphinylmethyl)methanes have been shown to serve as good phase-transfer catalysts which accelerate SN2 type displacements of octyl bromide with various nucleophiles (thiocyanate, cyanide, phenoxide, and thiolate) in solid-liquid two-phase systems.Alkylation of phenylacetonitrile with alkyl halides has also been carried out in liquid-liquid two-phase systems in the presence of the above sulphoxides to afford the corresponding mono-alkylated products in high yields.
