CAS 17429-36-6
:2-Cyclohexen-1-one, 4-methyl-4-phenyl-
Description:
2-Cyclohexen-1-one, 4-methyl-4-phenyl- is an organic compound characterized by its cyclic structure and the presence of both a ketone and an alkene functional group. It features a cyclohexene ring with a methyl group and a phenyl group attached to the same carbon, specifically at the 4-position. This compound is typically a colorless to pale yellow liquid with a distinctive odor. It is known for its reactivity due to the presence of the double bond, which can participate in various chemical reactions such as electrophilic additions. The ketone functionality contributes to its potential as a precursor in organic synthesis and its utility in the production of more complex molecules. Additionally, the presence of both the methyl and phenyl groups can influence its physical properties, such as boiling point and solubility. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if inhaled or ingested.
Formula:C13H14O
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 4 products.
6-Phenyl-6-methyl-1-cyclohexene-3-one
CAS:Formula:C13H14OPurity:95%Color and Shape:LiquidMolecular weight:186.24971-Methyl-2,3-dihydro-[1,1'-biphenyl]-4(1H)-one
CAS:<p>1-Methyl-2,3-dihydro-[1,1'-biphenyl]-4(1H)-one</p>Purity:98%Molecular weight:186.25g/mol1-Methyl-2,3-dihydro-[1,1'-biphenyl]-4(1H)-one
CAS:<p>1-Methyl-2,3-dihydro-[1,1'-biphenyl]-4(1H)-one is a chiral compound with an enolate functional group. It has been used to synthesize the lipase inhibitor ursodeoxycholic acid and cyclohexanones. The enzyme 1-methyl-2,3-dihydro-[1,1'-biphenyl]-4(1H)-one is able to catalyze the hydrolysis of esters and transesterification of esters. This class of compounds also has been found in pseudomonas fluorescens and has been shown to inhibit the growth of this bacteria.</p>Formula:C13H14OPurity:Min. 95%Molecular weight:186.26 g/mol



