709-08-0

Basic information

• Product Name: 4-(1-Cyclohexen-1-yl)phenol
• Synonyms: 4-(1-Cyclohexen-1-yl)phenol
• CAS NO: 709-08-0
• Molecular Formula: C₁₂H₁₄O
• Molecular Weight: 174.239
• Mol File: 709-08-0.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 304.6°Cat760mmHg
• Flash Point: 137.1°C
• Appearance: /
• Density: 1.086g/cm³
• Vapor Pressure: 0.000479mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: 4-(1-Cyclohexen-1-yl)phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1-Cyclohexen-1-yl)phenol(709-08-0)
• EPA Substance Registry System: 4-(1-Cyclohexen-1-yl)phenol(709-08-0)

Safety Data

• Hazardous Substances Data: 709-08-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h4,6-9,13H,1-3,5H2

Upstream product

• 843-55-0 1,1-bis(p-hydroxyphenyl)cyclohexane 
• 108-94-1 cyclohexanone 
• 108-95-2 phenol 
• 540-38-5 p-Iodophenol 
• 110-83-8 cyclohexene 
• 4203-50-3 2-phenoxytetrahydropyran 
• 1279062-76-8 1-[4-(tetrahydro-pyran-2-yloxy)-phenyl]-cyclohexanol 
• 1131-60-8 p-cyclohexylphenol 

Downstream Products

• 1131-60-8 p-cyclohexylphenol 
• 20758-60-5 1-(4-methoxyphenyl)cyclohexene 
• 613-36-5 4-cyclohexylanisole 
• 73761-76-9 4-cyclohexylphenyl acetate 
• 57328-06-0 4-[p-(1-cyclohexenyl)-phenoxy]-butyric acid 
• 38799-02-9 α-[p-(1-cyclohexenyl)-phenoxy]-decanoic acid ethyl ester 
• 38798-98-0 α-[p-(1-cyclohexenyl)-phenoxy]-dodecanoic acid ethyl ester 
• 38799-00-7 α-[p-(1-cyclohexenyl)-phenoxy]-undecanoic acid ethyl ester 

Relevant articles and documents

Discovery, Biocatalytic Exploration and Structural Analysis of a 4-Ethylphenol Oxidase from Gulosibacter chungangensis

The vanillyl-alcohol oxidase (VAO) family is a rich source of biocatalysts for the oxidative bioconversion of phenolic compounds. Through genome mining and sequence comparisons, we found that several family members lack a generally conserved catalytic aspartate. This finding led us to study a VAO-homolog featuring a glutamate residue in place of the common aspartate. This 4-ethylphenol oxidase from Gulosibacter chungangensis (Gc4EO) shares 42 % sequence identity with VAO from Penicillium simplicissimum, contains the same 8α-N3-histidyl-bound FAD and uses oxygen as electron acceptor. However, Gc4EO features a distinct substrate scope and product specificity as it is primarily effective in the dehydrogenation of para-substituted phenols with little generation of hydroxylated products. The three-dimensional structure shows that the characteristic glutamate side chain creates a closely packed environment that may limit water accessibility and thereby protect from hydroxylation. With its high thermal stability, well defined structural properties and high expression yields, Gc4EO may become a catalyst of choice for the specific dehydrogenation of phenolic compounds bearing small substituents.

SUBSTITUTED PHENOXYMETHYL DIHYDRO OXAZOLOPYRIMIDINONES, PREPARATION AND USE THEREOF

The present invention relates to a series of substituted phenoxymethyl dihydro oxazolopyrimidinones of formula (I) defined herein. This invention also relates to methods of making these compounds including novel intermediates. The compounds of this invent

Process for the production of monomeric alkenylphenols from dihydroxydiphenylalkanes

The invention relates to a process for the production of monomeric alkenylphenols from dihydroxydiphenylalkanes by thermal cleavage in certain solvents.