5078-75-1

Usage

Uses

Used in Chemical Production:
(3-Methylcyclopentyl)benzene is used as an intermediate in the synthesis of various chemicals, contributing to the development of new compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
(3-Methylcyclopentyl)benzene is used as a building block in the production of pharmaceuticals, aiding in the creation of new drugs and medications.
Used as a Solvent:
(3-Methylcyclopentyl)benzene is used as a solvent in various industrial processes, facilitating chemical reactions and improving the efficiency of manufacturing operations.
Used in Research and Development:
(3-Methylcyclopentyl)benzene is utilized in research and development settings to study its properties and explore its potential applications in new areas.
Note: It is important to handle (3-Methylcyclopentyl)benzene with care, as it is considered a hazardous substance and can cause skin and eye irritation.

Upstream product

• 18729-48-1 3-methylcyclopentanol 
• 71-43-2 benzene 
• 100-42-5 styrene 
• 21969-32-4 crotylmagnesium chloride 
• 96-37-7 methyl-cyclopentane 
• 622-24-2 2-phenylethyl chloride 
• 7446-70-0 aluminium trichloride 
• 107-05-1 3-chloroprop-1-ene 
• 177037-77-3 2-phenyl-5-hexen-1-ol 
• 110-82-7 cyclohexane 
• 1076-66-0 3-phenyl-1,5-hexadiene 
• 410098-30-5 [1-(iodomethyl)-4-pentenyl]benzene 
• 410098-31-6 [(2-phenylhex-5-enyl)seleno]benzene 
• 60-29-7 diethyl ether 

Downstream Products

• 65-85-0 benzoic acid 
• 64-19-7 acetic acid 

Relevant academic research and scientific papers

A tin hydride designed to facilitate removal of tin species from products of stannane-mediated radical reactions

The stannane 1, which is simple to prepare, behaves like the conventional reagents Bu3SnH and Ph3SnH in standard free radical reactions, but with the special characteristic that the tin-containing byproducts are easily and very largely removed by mild hydrolysis (LiOH-water-THF or TsOH-water-THF), which converts them into base-soluble (aqueous NaHCO3) materials. The performance of stannane 1 was evaluated for a range of radical reactions involving halides, selenides, Barton-McCombie deoxygenation, and enyne cyclization. In several cases the effectiveness of the workup procedure in removing tin species was monitored by 1H NMR.

Stereochemistry of the thermal isomerizations of (1/R,2R)-1-((E)-Styryl)-2-methylcyclopropane to 3-phenyl-4-methylcyclopentenes

(1A,2R)-1-((E)-Styryl)-2-methylcyclopropane at 250 °C racemizes and isomerizes to 6-phenylhexa-1,4-(Z)-diene and to the four isomers of 3-phenyl-4-methylcyclopentene. From the measured rate constants for racemization and for structural isomerizations, and

Acid-catalyzed Reactions of Aromatic Hydrocarbons with Alkanes and Cycloalkanes. X. Alkylations with Cyclohexane

The complex reaction mixtures of the nonconventional alkylation of benzene with cyclohexane in the presence of Lewis/proton acids and promotors were investigated by gas-liquid chromatography and mass spectrometry.Four representative groups of hydrocarbons were found including cycloalkylbenzenes, substituted indanes or tetralines (C12H16), C1-C6-alkylbenzenes and isomeric biscycloalkyls (C12H22).Their formation is interpreted as a competition between alkylation, (without or with isomerization), ringfission with cycloalkylation or fragmentation, and self-alkylation; phenylcycloalkylcations and phenylalkylcations are the intermediates.