7334-52-3

Basic information

• Product Name: [bis(ethylsulfanyl)methyl]benzene
• Synonyms: [Bis(ethylsulfanyl)methyl]benzene; benzene, [bis(ethylthio)methyl]-
• CAS NO: 7334-52-3
• Molecular Formula: C₁₁H₁₆S₂
• Molecular Weight: 212.3747
• Mol File: 7334-52-3.mol
• Article Data: 40

Chemical Properties

• Boiling Point: 291.4°C at 760 mmHg
• Flash Point: 123.7°C
• Density: 1.059g/cm³
• Vapor Pressure: 0.00341mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: [bis(ethylsulfanyl)methyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: [bis(ethylsulfanyl)methyl]benzene(7334-52-3)
• EPA Substance Registry System: [bis(ethylsulfanyl)methyl]benzene(7334-52-3)

Safety Data

• Hazardous Substances Data: 7334-52-3(Hazardous Substances Data)

Usage

Description

[bis(ethylsulfanyl)methyl]benzene, with the molecular formula C14H20S2, is a colorless liquid characterized by a distinct and pungent odor. This chemical compound serves as a versatile intermediate in the production of other chemicals and is a common starting material for the synthesis of various organic compounds. It is also recognized for its potential use as a chemical reagent in organic synthesis and as a solvent in chemical processes. Furthermore, [bis(ethylsulfanyl)methyl]benzene has demonstrated biological activity, leading to investigations into its possible pharmacological applications.

Uses

Used in Chemical Synthesis:
[bis(ethylsulfanyl)methyl]benzene is used as an intermediate in the chemical synthesis industry for the production of other chemicals. Its unique structure and properties make it a valuable component in creating a wide range of chemical products.
Used in Organic Synthesis:
In the field of organic synthesis, [bis(ethylsulfanyl)methyl]benzene is utilized as a starting material for synthesizing various organic compounds. Its reactivity and functional groups contribute to the formation of complex molecules with specific applications.
Used as a Chemical Reagent:
[bis(ethylsulfanyl)methyl]benzene is employed as a chemical reagent in organic synthesis, where it aids in the formation of new chemical bonds and the transformation of other molecules.
Used as a Solvent in Chemical Processes:
[bis(ethylsulfanyl)methyl]benzene also serves as a solvent in various chemical processes, facilitating reactions and improving the efficiency of the overall process.
Used in Pharmaceutical Research:
[bis(ethylsulfanyl)methyl]benzene has been studied for its potential pharmacological applications due to its demonstrated biological activity. Researchers are exploring its potential use in the development of new drugs and therapies.
Used in the Chemical Industry:
Overall, [bis(ethylsulfanyl)methyl]benzene is a significant chemical compound with a wide range of potential uses across various industries, including chemical synthesis, organic synthesis, pharmaceutical research, and more. Its versatility and importance in these fields make it a valuable asset in the development of new products and technologies.

Upstream product

• 688-62-0 triethyl trithiophosphite 
• 100-52-7 benzaldehyde 
• 623-49-4 ethyl cyanoformate 
• 75-08-1 ethanethiol 
• 169172-96-7 α-Methoxy-α-(ethylthio)toluene 
• 24850-33-7 allyltributylstanane 
• 1125-88-8 benzaldehyde dimethyl acetal 
• 1612786-69-2 ethyl(phenyl(2,4,6-trimethoxyphenyl)methyl)sulfane 
• 100-39-0 benzyl bromide 
• 625-60-5 ethyl thioacetate 
• 70770-06-8 1-benzyloxy-3-phenylpropane 
• 936-51-6 2-phenyl-1,3-dioxolane 
• 81375-98-6 4,4-bis(ethylsulfanyl)but-3-en-2-one 
• 2168-78-7 methyl dithiobenzoate 

Downstream Products

• 5425-44-5 2-Phenyl-[1,3]dithiane 
• 14316-85-9 α.β-Bis-ethylmercapto-β-phenyl-propionsaeure-ethylester 
• 3462-48-4 1-Phenyl-pentan-1-on-bis-ethylthioacetal 
• 897-78-9 2,6-bis(phenylmethylene)cyclohexanone 
• 92861-26-2 sek-Butylphenylketon-diethyldithioketal 
• 29776-05-4 1-<α-(ethylthio)benzyl>-4-methoxybenzene 
• 7500-76-7 4,4'-dimethoxytriphenylmethane 
• 29775-96-0 3-((ethylthio)(phenyl)methyl)pentane-2,4-dione 
• 29776-01-0 (α-Aethylmercapto-benzyl)-malonsaeure-diaethylester 
• 60340-31-0 Ethylsulfanyl-phenyl-acetonitrile 
• 107006-49-5 2-(Ethylsulfanyl-phenyl-methyl)-cyclohexanone 
• 91475-92-2 (1,1-Bis-ethylsulfanyl-but-3-enyl)-benzene 
• 22914-06-3 acetophenone diethyldithioacetal 
• 103-30-0 (E)-1,2-diphenyl-ethene 

Relevant articles and documents

Neighboring-Group Participation in the Gas Phase. Loss of Benzaldehyde from dialkylsilyl-Substituted 1,3-Dithianes

dialkylsilyl-substituted 1,3-dithianes show in CI-MS an abundant loss of benzaldehyde from the (1+) quasi-molecular ion.The fragmentation is explained with an intramolecular redox process, where a hydride is proposed to be transfer

Cyanuric chloride-catalyzed thioacetalization for organocatalytic synthesis of thioacetals

The thioacetalization of aromatic aldehydes has been realized with broad diversity in the presence of various thiols and thiophenols using cyanuric chloride as an organocatalyst.

Reductive Alkylation of Arenes by a Thiol-Based Multicomponent Reaction

A simple and highly chemo- and regioselective method for introducing primary alkyl substituents into aromatic compounds was developed. The method is based on an electrophilic aromatic substitution of an aldehyde, promoted by a thiol, to afford 1-(alkylthio)alkylarenes, which can either be reduced in situ with triethylsilane or reacted further. This multicomponent reaction enables the direct introduction of both aromatic and linear and branched aliphatic alkyl groups into arenes. The above one-pot protocol may be performed in air and in the presence of water and is compatible with various functional groups.