5418-20-2 Usage
Description
([(benzylsulfanyl)(phenyl)methyl]sulfanylmethyl)benzene is a complex organic molecule characterized by its intricate structure that features a central benzene ring with two benzylsulfanyl groups attached to it. Each of these groups is further connected to a phenylmethylsulfanyl group, creating a highly branched and multifunctional compound with multiple sulfur and aromatic carbon groups. This unique arrangement of atoms suggests potential applications in various fields, particularly in organic synthesis and the development of innovative materials.
Uses
Used in Organic Synthesis:
([(benzylsulfanyl)(phenyl)methyl]sulfanylmethyl)benzene is utilized as a key intermediate in organic synthesis for the creation of a variety of complex organic compounds. Its unique structure, with multiple sulfur and aromatic carbon groups, allows for versatile chemical reactions and the formation of a wide range of products.
Used in Material Science:
In the field of material science, ([(benzylsulfanyl)(phenyl)methyl]sulfanylmethyl)benzene is employed as a building block for the development of new materials. Its complex molecular structure and the presence of sulfur and aromatic carbon groups make it a promising candidate for the synthesis of advanced materials with specific properties, such as improved thermal stability, electrical conductivity, or chemical resistance.
Used in Pharmaceutical Industry:
([(benzylsulfanyl)(phenyl)methyl]sulfanylmethyl)benzene is used as a precursor in the pharmaceutical industry for the synthesis of potential drug candidates. Its complex structure and the presence of sulfur and aromatic carbon groups can be leveraged to design molecules with specific biological activities, targeting various therapeutic areas.
Used in Chemical Research:
In chemical research, ([(benzylsulfanyl)(phenyl)methyl]sulfanylmethyl)benzene serves as a model compound for studying the properties and reactivity of complex organic molecules. Its unique structure provides opportunities for investigating various chemical reactions and understanding the underlying mechanisms, which can contribute to the advancement of organic chemistry and related fields.
Check Digit Verification of cas no
The CAS Registry Mumber 5418-20-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,1 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5418-20:
(6*5)+(5*4)+(4*1)+(3*8)+(2*2)+(1*0)=82
82 % 10 = 2
So 5418-20-2 is a valid CAS Registry Number.
5418-20-2Relevant articles and documents
Direct Synthesis of Unsymmetrical Dithioacetals
Bognar, Sabine,van Gemmeren, Manuel
supporting information, p. 4859 - 4863 (2021/02/03)
Dithioacetals are a frequently used motif in synthetic organic chemistry and have recently seen increasing attention as structural motif in promising antiviral agents against plant pathogens. Most existing reports, however, only discuss symmetrical dithioacetals. Examples of mixed dithioacetals are scarce and no general method for the selective synthesis of these compounds exists. Herein, a synthetically simple general one-step protocol was developed for the synthesis of a broad range of unsymmetrical dithioacetals consisting of one aromatic and one aliphatic thiol moiety from the corresponding aldehyde/thiol mixture. The mixed S,S-acetals were obtained in high yields, and a great variety of functional groups was tolerated. Kinetic control enabled an excellent selectivity in regard to the unsymmetrical dithioacetal.
An expeditious and efficient bromomethylation of thiols: Enabling bromomethyl sulfides as useful building blocks
Silva-Cuevas, Carolina,Paleo, Ehecatl,León-Rayo, David F.,Lujan-Montelongo, J. Armando
, p. 24654 - 24659 (2018/07/25)
A facile and highly efficient method for the bromomethylation of thiols, using paraformaldehyde and HBr/AcOH, has been developed, which advantageously minimizes the generation of highly toxic byproducts. The preparation of 22 structurally diverse α-bromomethyl sulfides illustrates the chemo-tolerant applicability while bromo-lithium exchange and functionalization sequences, free radical reductions, and additions of the title compounds demonstrate their synthetic utility.
Chemoselective and odorless transthioacetalization of acetals using α-oxo-ketene dithioacetals as thiol equivalents
Yu, Hai-Feng
, p. 1280 - 1286 (2013/04/10)
Using α-oxo-ketene dithioacetals 1a as odorless thiol equivlents, an efficient and odorless transthioacetalization of acetals 2 has been developed. In the presence of MeCOCl in MeOH, the cleavage of 1a commences to generate thiols at both room and reflux temperatures, and the generated thiols then react with acetals 2 to give correspecting thioacetals 3 in good yield. This transthioacetalization is characterized by mild reaction conditions, simple procedure, good yields, and perfect chemoselectivity. It is noteworthy that only a very faint odor of thiols can be perceived during both the reaction and workup.