CAS 5442-00-2

2-Cyclohexyl-1-propanol

Description:

2-Cyclohexyl-1-propanol is an organic compound characterized by its cyclohexyl and propanol functional groups. It features a cyclohexyl ring attached to a propanol chain, which contributes to its unique properties. This compound is typically a colorless to pale yellow liquid with a characteristic odor. It is moderately soluble in water, with better solubility in organic solvents such as ethanol and ether. The presence of both a cyclohexyl group and a hydroxyl (-OH) group influences its reactivity, making it a potential candidate for various chemical reactions, including oxidation and esterification. Additionally, 2-cyclohexyl-1-propanol can exhibit hydrophobic characteristics due to the cyclohexyl moiety, affecting its interactions in biological systems and industrial applications. Its applications may extend to the synthesis of pharmaceuticals, fragrances, and as a solvent in organic chemistry. Safety data indicates that, like many alcohols, it should be handled with care, as it may cause irritation upon contact with skin or eyes.

Formula: C₉H₁₈O

InChI: InChI=1S/C9H18O/c1-8(7-10)9-5-3-2-4-6-9/h8-10H,2-7H2,1H3

InChI key: InChIKey=IRIVQXLOJHCXIE-UHFFFAOYSA-N

SMILES: C(CO)(C)C1CCCCC1

Synonyms:

• 2-Cyclohexyl-1-propanol
• 2-Cyclohexylpropanol
• Cyclohexaneethanol, beta-methyl-
• Cyclohexaneethanol, β-methyl-
• Nsc 20786
• β-Methylcyclohexaneethanol
• 2-Cyclohexylpropan-1-ol

2-Cyclohexyl-1-propanol

CAS: 5442-00-2

Formula: C₉H₁₈O

Purity: 95%

Molecular weight: 142.2386

Ref: IN-DA00DDQR

2-Cyclohexylpropan-1-ol

CAS: 5442-00-2

2-Cyclohexylpropan-1-ol

Purity: 97%

Molecular weight: 142.24g/mol

Ref: 54-OR1044024

2-Cyclohexylpropan-1-ol

CAS: 5442-00-2

Purity: 95.0%

Color and Shape: Liquid

Molecular weight: 142.24200439453125

Ref: 10-F239818

2-Cyclohexyl-1-propanol

CAS: 5442-00-2

2-Cyclohexyl-1-propanol (2CYP) is a chemical compound that is an alkali metal. It can be used to remove the sulfate from benzyl alcohol, which is a precursor in the production of polystyrene. 2CYP is also used as a catalyst for the hydrogenation of alkenes and alkynes to produce hydrogenated hydrocarbons. The elucidation of the mechanism by which 2CYP reduces sulfate has been shown to involve two steps: dehydrogenation of 2CYP followed by addition of sulfate to form elemental sulfur. In environmental health, 2CYP has been shown to reduce chloride levels and was found to be more effective than sodium hydroxide or sodium chloride.
2CYP also reduces levels of lead and cadmium in water samples.

Formula: C₉H₁₈O

Purity: Min. 95%

Molecular weight: 142.24 g/mol

Ref: 3D-FAA44200