CAS 17264-02-7
:1-Cyclohexyl-1-propanol
Description:
1-Cyclohexyl-1-propanol, with the CAS number 17264-02-7, is an organic compound characterized by its cyclohexyl and propanol functional groups. It is a colorless to pale yellow liquid at room temperature, exhibiting a moderate viscosity. The compound is known for its pleasant odor, which can be reminiscent of floral or fruity notes, making it potentially useful in fragrance formulations. Its molecular structure includes a cyclohexyl group attached to a propanol moiety, contributing to its unique chemical properties. 1-Cyclohexyl-1-propanol is relatively soluble in organic solvents but has limited solubility in water due to its hydrophobic cyclohexyl ring. The compound may participate in various chemical reactions typical of alcohols, such as oxidation and esterification. Additionally, it may exhibit moderate toxicity, necessitating proper handling and safety precautions in laboratory and industrial settings. Overall, 1-cyclohexyl-1-propanol is of interest in both synthetic organic chemistry and potential applications in the fragrance industry.
Formula:C9H18O
InChI:InChI=1S/C9H18O/c1-2-9(10)8-6-4-3-5-7-8/h8-10H,2-7H2,1H3
InChI key:InChIKey=JVTXOMXEPFDMHB-UHFFFAOYSA-N
SMILES:C(CC)(O)C1CCCCC1
Synonyms:- (1S)-1-cyclohexylpropan-1-ol
- 1-Cyclohexylpropan-1-Ol
- 1-Cyclohexylpropanol
- 1-Cyclohexylpropanol-1
- Alpha-Ethyl-Cyclohexanemethano
- Alpha-Ethylcyclohexane-1-Methanol
- Cyclohexanemethanol, α-ethyl-
- Cyclohexyl ethyl carbinol
- Ethylcyclohexylcarbinol
- NSC 95429
- α-Ethylcyclohexanemethanol
- See more synonyms
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Found 2 products.
1-Cyclohexyl-1-propanol
CAS:<p>1-Cyclohexyl-1-propanol is an organic compound that is a colorless liquid with a sweet, etherial odor. It has been used in pharmaceutical preparations as a solvent and as an intermediate for the production of other compounds. 1-Cyclohexyl-1-propanol has been shown to have effects on the bladder muscle and detrusor muscle, which may be due to its ability to inhibit the activity of amines. The compound also forms enantiomers, which are stereoselective and react differently in multiphase reactions.</p>Formula:C9H18OPurity:Min. 95%Molecular weight:142.24 g/mol

