7570-92-5

Basic information

• Product Name: (cyclohexylsulfanyl)benzene
• Synonyms: (Cyclohexylsulfanyl)benzene; benzene, (cyclohexylthio)-; Cyclohexyl phenyl sulfide
• CAS NO: 7570-92-5
• Molecular Formula: C₁₂H₁₆S
• Molecular Weight: 192.3204
• Mol File: 7570-92-5.mol
• Article Data: 94

Chemical Properties

• Boiling Point: 293.6°C at 760 mmHg
• Flash Point: 127.5°C
• Density: 1.04g/cm³
• Vapor Pressure: 0.00299mmHg at 25°C
• Refractive Index: 1.569
• CAS DataBase Reference: (cyclohexylsulfanyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (cyclohexylsulfanyl)benzene(7570-92-5)
• EPA Substance Registry System: (cyclohexylsulfanyl)benzene(7570-92-5)

Safety Data

• Hazardous Substances Data: 7570-92-5(Hazardous Substances Data)

Usage

Description

(Cyclohexylsulfanyl)benzene, also known as thiophenol, is a chemical compound that features a benzene ring with a sulfur atom and a cyclohexyl group attached. It is characterized as a colorless liquid with a strong, unpleasant odor and is recognized for its applications in various industries due to its unique chemical properties.

Uses

Used in Chemical Synthesis:
(Cyclohexylsulfanyl)benzene is used as a building block in the chemical synthesis industry for creating a wide range of products. Its unique structure allows it to be a versatile component in the development of new compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (cyclohexylsulfanyl)benzene is utilized as a key component in the production of various drugs. Its chemical properties make it a valuable asset in the synthesis of medicinal compounds.
Used in Dye Manufacturing:
(Cyclohexylsulfanyl)benzene is employed as a crucial ingredient in the manufacturing of dyes. Its chemical structure contributes to the color and stability of the dyes produced.
Used in Pesticide and Fungicide Formulation:
(cyclohexylsulfanyl)benzene is also used as an active ingredient in the formulation of insecticides and fungicides. Its properties help in controlling and preventing the growth of pests and fungi that can damage crops and other plants.
Used in Organic Synthesis as a Reagent:
(Cyclohexylsulfanyl)benzene serves as a reagent in organic synthesis, facilitating various chemical reactions and contributing to the formation of desired products.
Caution:

Upstream product

• 108-85-0 1-bromocyclohexane 
• 930-69-8 sodium thiophenolate 
• 108-98-5 thiophenol 
• 110-83-8 cyclohexene 
• 14204-24-1 N-(phenylthio)succinimide 
• 108-93-0 cyclohexanol 
• 4922-47-8 1-(phenylthio)cyclohex-1-ene 
• 37457-08-2 cyclohexane-1,1-diylbis(phenylsulfane) 
• 108-94-1 cyclohexanone 
• 882-33-7 diphenyldisulfane 
• 626-62-0 Cyclohexyl iodide 
• 24371-94-6 cyclohexylmercury chloride 
• 1564-39-2 1-oxa-4-thiaspiro-<4,5>decan-2-one 
• 71-43-2 benzene 

Downstream Products

• 6947-57-5 cyclohexyl phenyl sulfone 
• 3324-82-1 (phenylsulfinyl)cyclohexane 
• 100971-72-0 1-(4-cyclohexylmercapto-phenyl)-ethanone 
• 132-65-0 dibenzothiophene 
• 1569-69-3 Cyclohexanethiol 
• 874-79-3 phenyl(propyl)sulfide 
• 622-38-8 Ethyl phenyl sulfide 
• 139-66-2 diphenyl sulfide 
• 882-33-7 diphenyldisulfane 
• 1126-80-3 (n-butylthio)benzene 
• 100-68-5 methyl-phenyl-thioether 
• 1129-70-0 pentyl phenyl sulfide 
• 4922-47-8 1-(phenylthio)cyclohex-1-ene 
• 110-82-7 cyclohexane 

Relevant articles and documents

Base-Mediated Radical Borylation of Alkyl Sulfones

A practical and direct method was developed for the production of versatile alkyl boronate esters via transition metal-free borylation of primary and secondary alkyl sulfones. The key to the success of the strategy is the use of bis(neopentyl glycolato) diboron (B2neop2), with a stoichiometric amount of base as a promoter. The practicality and industrial potential of this protocol are highlighted by its wide functional group tolerance, the late-stage modification of complex compounds, no need for further transesterification, and operational simplicity. Radical clock, radical trap experiments, and EPR studies were conducted which show that the borylation process involves radical intermediates.

Synthesis method of alkyl sulfide compound

The invention belongs to the technical field of synthesis of organic compounds, and provides a novel method for preparing an alkyl sulfide compound. According to the method, direct synthesis preparation of the thioether compound is realized by utilizing direct coupling of an organic sulfinic acid compound and alkane under acid and illumination conditions. According to the present invention, the alkane C-H bond direct thioetherification method is adopted, the reaction functional group does not need to be configured in advance, the thioether compound synthesis reaction steps are substantially shortened, the raw materials are cheap and easily available, the conditions are mild and green, the operation is simple, convenient and safe, and the good economic prospect is provided.

Visible-Light-Mediated Alkylation of Thiophenols via Electron Donor-Acceptor Complexes Formed between Two Reactants

A metal-free, photocatalyst-free, photochemical system was developed for the direct alkylation of thiophenols via electron donor-acceptor (EDA) complexes (KEDA = 145 M-1) between two reactants, N-hydroxyphthalimide esters as acceptors and thiophenol anions as donors, in the presence of a tertiary amine. The EDA complexes in the reaction system have a broad range of visible-light absorption (400-650 nm) and can trigger the reaction effectively under sunlight.