2883-12-7

Basic information

• Product Name: 1-Phenyl-3-cyclopentylpropane
• Synonyms: (3-Cyclopentylpropyl)benzene;1-Phenyl-3-cyclopentylpropane
• CAS NO: 2883-12-7
• Molecular Formula: C₁₄H₂₀
• Molecular Weight: 188.3086
• Mol File: 2883-12-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 258.34°C (rough estimate)
• Flash Point: 112.7°C
• Appearance: /
• Density: 0.9233
• Vapor Pressure: 0.00987mmHg at 25°C
• Refractive Index: 1.5130
• CAS DataBase Reference: 1-Phenyl-3-cyclopentylpropane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Phenyl-3-cyclopentylpropane(2883-12-7)
• EPA Substance Registry System: 1-Phenyl-3-cyclopentylpropane(2883-12-7)

Safety Data

• Hazardous Substances Data: 2883-12-7(Hazardous Substances Data)

Usage

Type of compound

Cyclic alkane with a phenyl substituent and a cyclopentyl group.

Unique structure

Combination of a phenyl group and a cyclopentyl group in a propane chain.

Synthesis use

Building block for the synthesis of various pharmaceuticals and other organic compounds.

Research potential

Studied for its potential use as a precursor in the production of new materials and as a reagent in organic synthesis.

Applications

Potential applications in the field of medicinal chemistry, drug development, and other industries due to its unique chemical structure and properties.

InChI:InChI=1/C14H20/c1-2-7-13(8-3-1)11-6-12-14-9-4-5-10-14/h1-3,7-8,14H,4-6,9-12H2

Upstream product

• 134949-06-7 (3-(cyclopent-1-en-1-yl)propyl)benzene 
• 104-52-9 phenylpropyl chloride 
• 137-43-9 Cyclopentyl bromide 
• 1392140-96-3 5,5-dimethyl-2-(3-phenylpropyl)-1,3,2-dioxaborinane 
• 637-59-2 1-Bromo-3-phenylpropane 
• 122-97-4 3-Phenyl-1-propanol 
• 69804-99-5 3-phenylpropanol methanesulfonate 
• 1462-75-5 3-phenylpropylmagnesium bromide 
• 120-92-3 cyclopentanone 
• 53668-63-6 1-hydroxy-1-(3-phenyl-propyl)-cyclopentane 
• 180286-97-9 9-(3-phenylpropyl)-9-borabicyclo[3.3.1]nonane 
• 64-17-5 ethanol 
• 2883-07-0 1-cyclohexyl-3-cyclopentyl-propane 
• 3558-06-3 cyclopentyl tosylate 

Downstream Products

• 2883-07-0 1-cyclohexyl-3-cyclopentyl-propane 
• 2189-60-8 Octylbenzene 

Relevant articles and documents

Iron-Based Catalyst for Borylation of Unactivated Alkyl Halides without Using Highly Basic Organometallic Reagents

The mild borylation of alkyl bromides and chlorides with bis(neopentylglycolato)diborane (B2neop2) mediated by iron-bis amide is described. The reaction proceeds with a broad substrate scope and good functional group compatibility. Moreover, sufficient ca

NHC-copper hydrides as chemoselective reducing agents: Catalytic reduction of alkynes, alkyl triflates, and alkyl halides

The NHC-copper-catalyzed Z-selective semi-reduction of terminal and internal alkynes, as well as the NHC-copper-catalyzed reduction of primary alkyl triflates and primary and secondary alkyl iodides and bromides are described. The high chemoselectivity demonstrated in these examples illustrates the mild nature of copper hydride complexes as reducing agents, which have applications in synthetic chemistry beyond their traditional role in the reduction of activated alkenes and carbonyl compounds.

Silver-catalyzed cross-coupling reactions of alkyl bromides with alkyl or aryl Grignard reagents

Treatment of secondary or tertiary alkyl bromides with alkyl Grignard reagents in the presence of catalytic amounts of silver bromide and potassium fluoride in CH2Cl2 afforded the corresponding cross-coupling products in reasonable yields. Moreover, silver showed catalytic activity for the cross-coupling reactions of alkyl bromides with aryl Grignard reagents.