6627-84-5

Basic information

• Product Name: 4-CYCLOPENT-2-EN-1-YLPHENOL
• Synonyms: 4-CYCLOPENT-2-EN-1-YLPHENOL;IFLAB-BB F0701-0018;4-Cyclopent-2-enyl-phenol
• CAS NO: 6627-84-5
• Molecular Formula: C₁₁H₁₂O
• Molecular Weight: 160.21
• Mol File: 6627-84-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 64-65 °C(Solv: ligroine (8032-32-4))
• Boiling Point: 282.7°Cat760mmHg
• Flash Point: 127.1°C
• Appearance: /
• Density: 1.107g/cm³
• Vapor Pressure: 0.00193mmHg at 25°C
• Refractive Index: 1.592
• PKA: 10.10±0.30(Predicted)
• CAS DataBase Reference: 4-CYCLOPENT-2-EN-1-YLPHENOL(CAS DataBase Reference)
• NIST Chemistry Reference: 4-CYCLOPENT-2-EN-1-YLPHENOL(6627-84-5)
• EPA Substance Registry System: 4-CYCLOPENT-2-EN-1-YLPHENOL(6627-84-5)

Safety Data

• Hazardous Substances Data: 6627-84-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C11H12O/c12-11-7-5-10(6-8-11)9-3-1-2-4-9/h1,3,5-9,12H,2,4H2

Upstream product

• 542-92-7 cyclopenta-1,3-diene 
• 108-95-2 phenol 
• 15131-55-2 di-2-cyclopenten-1-yl ether 
• 108-88-3 toluene 
• 80-05-7 BPA 

Downstream Products

• 1518-83-8 4-cyclopentylphenol 
• 877-46-3 4-(1-cyclopenten-1-yl)phenol 
• 103983-63-7 trans-4-Cyclopentyl-cyclohexanol 
• 103983-63-7 cis-4-Cyclopentyl-cyclohexanol 
• 105886-88-2 4-Cyclopent-1-enyl-2-(4-o-tolyl-piperazin-1-ylmethyl)-phenol 
• 88737-67-1 ethyl α-acetate 
• 105886-85-9 4-(cyclopent-2-en-1-yl)-2-(N,N-dimethylaminomethyl)phenol 
• 105886-86-0 4-Cyclopent-2-enyl-2-diethylaminomethyl-phenol 
• 105886-89-3 3-chloro-1-propane 
• 88737-64-8 3-prop-1-ene 
• 88737-61-5 β-propionitrile 
• 88737-62-6 α-acetic acid 
• 88737-66-0 3-bromo-1-propane 
• 105886-90-6 1,3-bispropane 

Relevant articles and documents

METHOD OF PRODUCING FIVE-CARBON RING-CONTAINING COMPOUND AND FIVE-CARBON RING DERIVATIVE-CONTAINING POLYURETHANE, AND FIVE-CARBON RING DERIVATIVE-CONTAINING POLYURETHANE

A method of producing a five-carbon ring derivative-containing polyurethane involves introducing a DCPD-derived 5-carbon cyclic compound into a polyurethane material and effectuating polymerization in the presence of a solvent of a low boiling point and l

Alkylation of phenol with olefins in the presence of lignosulfonic acids

Alkylation of phenol with cyclohexene, 1-octene, dicyclopentadiene, 1,3-cyclopentadiene, and butylene polymer distillate at 100-140°C was studied. The process was performed in the presence of lignosulfonic acids obtained from industrial calcium lignosulfonates.

INDIRECT HYDROXYLATION OF PHENOLS: A NEW ROUTE TO HYDROQUINONES

Hydroquinone and alkyl hydroquinones are obtained from the corresponding phenols by alkylation with cyclopentadiene followed by isomerization and oxidation.