CAS 5437-46-7
:4-Phenylcyclohexanol
Description:
4-Phenylcyclohexanol is an organic compound characterized by a cyclohexane ring substituted with a phenyl group and a hydroxyl group (–OH) at the 4-position. Its molecular formula is C12H16O, indicating it is a secondary alcohol. This compound typically appears as a colorless to pale yellow liquid with a characteristic odor. It is relatively soluble in organic solvents but has limited solubility in water due to its hydrophobic cyclohexane structure. 4-Phenylcyclohexanol exhibits moderate polarity, which influences its reactivity and interactions with other substances. It can participate in various chemical reactions, including oxidation and esterification, making it useful in organic synthesis and as an intermediate in the production of pharmaceuticals and fragrances. Additionally, it may exhibit chiral properties, leading to potential applications in asymmetric synthesis. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper safety protocols should be followed when working with this substance in laboratory settings.
Formula:C12H16O
InChI:InChI=1S/C12H16O/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-5,11-13H,6-9H2
InChI key:InChIKey=YVVUSIMLVPJXMY-UHFFFAOYSA-N
SMILES:OC1CCC(CC1)C2=CC=CC=C2
Synonyms:- 4-Phenyl-1-cyclohexanol
- 4-Phenylcyclohexan-1-ol
- Ai3-12031
- Cyclohexanol, 4-phenyl-
- NSC 16118
- NSC 17139
- 4-Phenylcyclohexanol
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Found 4 products.
4-Phenyl-cyclohexanol
CAS:4-Phenyl-cyclohexanolPurity:95%Color and Shape:SolidMolecular weight:176.25g/mol4-Phenyl-cyclohexanol
CAS:<p>4-Phenyl-cyclohexanol is a cyclohexane ring with a hydroxyl group on it. It is an aromatic hydrocarbon and can be found in many natural products, such as naphthalene, carbonyl group, geometric isomers, c–h bond. 4-Phenyl-cyclohexanol has been shown to have synergic effects when combined with other compounds, such as furyl and isopropylbenzyl alcohol. It has been isolated from the fungus Myrothecium verrucaria and also produced by enzymatic conversion of phenol. 4-Phenyl-cyclohexanol can be used to reduce ferredoxin to ferrodoxin and form NADPH in the biosynthesis of aromatic amino acids.</p>Formula:C12H16OPurity:Min. 95%Molecular weight:176.26 g/mol



