89654-30-8

Basic information

• Product Name: [(2-phenylcyclopropyl)sulfonyl]benzene
• CAS NO: 89654-30-8
• Molecular Formula: C₁₅H₁₄O₂S
• Molecular Weight: 258.3355
• Mol File: 89654-30-8.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 449.5°C at 760 mmHg
• Flash Point: 282.7°C
• Density: 1.262g/cm³
• Vapor Pressure: 7.59E-08mmHg at 25°C
• Refractive Index: 1.622
• CAS DataBase Reference: [(2-phenylcyclopropyl)sulfonyl]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: [(2-phenylcyclopropyl)sulfonyl]benzene(89654-30-8)
• EPA Substance Registry System: [(2-phenylcyclopropyl)sulfonyl]benzene(89654-30-8)

Safety Data

• Hazardous Substances Data: 89654-30-8(Hazardous Substances Data)

Usage

Description

[(2-phenylcyclopropyl)sulfonyl]benzene is a chemical compound characterized by the molecular formula C18H16O2S. It is a white solid that is insoluble in water and is known for its unique properties and reactivity due to the presence of a sulfonyl group attached to a phenylcyclopropyl ring. [(2-phenylcyclopropyl)sulfonyl]benzene is primarily utilized in organic synthesis and serves as a valuable building block in the field of organic chemistry.

Uses

Used in Pharmaceutical Synthesis:
[(2-phenylcyclopropyl)sulfonyl]benzene is used as a reactive intermediate for the synthesis of various pharmaceuticals. Its sulfonyl group, being a strong electron-withdrawing group, contributes to its utility in chemical reactions, making it a crucial component in the development of new drugs.
Used in Agrochemical Synthesis:
Similarly, in the agrochemical industry, [(2-phenylcyclopropyl)sulfonyl]benzene is employed as a key intermediate in the synthesis of different agrochemicals. Its unique structure and properties enable the creation of novel compounds with potential applications in agriculture.
Used in Organic Chemistry Research:
[(2-phenylcyclopropyl)sulfonyl]benzene is also used as a building block in organic chemistry research. Its distinct properties make it an interesting subject for studying various chemical reactions and exploring new synthetic pathways. This contributes to the advancement of knowledge in organic chemistry and the development of innovative chemical processes.

Upstream product

• 1228297-54-8 3-chloro-3-phenyl-propyl phenyl sulfone 
• 104-87-0 4-methyl-benzaldehyde 
• 104-88-1 4-chlorobenzaldehyde 
• 100-52-7 benzaldehyde 
• 123-11-5 4-methoxy-benzaldehyde 
• 630-19-3 pivalaldehyde 
• 104-55-2 3-phenyl-propenal 
• 100-42-5 styrene 
• 7205-91-6 phenylthiomethyl chloride 
• 58688-13-4 cis-2-phenyl-1-(phenylthio)cyclopropane 
• 873-55-2 sodium benzenesulfonate 
• 637-59-2 1-Bromo-3-phenylpropane 
• 17494-61-0 ((3-phenylpropyl)sulfonyl)benzene 
• 960-41-8 (E)-1-phenyl-3-(phenylsulfonyl)prop-2-en-1-one 

Relevant articles and documents

Synthesis of substituted tetrahydrofurans via intermolecular reactions of γ-chlorocarbanions of 3-substituted 3-chloro-propylphenyl sulfones with aldehydes

Carbanions of 3-substituted-3-chloropropyl phenyl sulfones add to carbonyl groups of aldehydes to produce aldol type adducts that undergo 1,5-intramolecular substitution giving 2,3,5-trisubstituted tetrahydrofurans. The effect of substituents in the 3-pos

Improved dimethylsulfoxonium methylide cyclopropanation procedures, including a tandem oxidation variant

A new procedure for the cyclopropanation of α,β-unsaturated carbonyl compounds and related systems is described which employs trimethylsulfoxonium iodide and an organic base in acetonitile to generate dimethylsulfoxonium methylide in situ; in addition, pr

Phase transfer catalyzed cyclopropanation of trans-styryl aryl sulfones with dimethyl sulfoxonium methylide

Some new trans-aryl cyclopropyl sulfones (II) have been prepared by the cycloaddition of dimethylsulfoxonium methylide to trans-styryl aryl sulfones (I) by two different methods. It is observed that the reaction in presence of a phase transfer catalyst proceeds in a facile manner.