CAS 705-73-7
:α-Propylbenzeneethanol
Description:
α-Propylbenzeneethanol, with the CAS number 705-73-7, is an organic compound characterized by its structure, which features a propyl group attached to a benzene ring, with a hydroxyl (-OH) group indicating its classification as an alcohol. This compound typically appears as a colorless to pale yellow liquid and is known for its aromatic properties due to the presence of the benzene ring. It has a moderate boiling point and is soluble in organic solvents, while its solubility in water is limited. α-Propylbenzeneethanol is often used in the synthesis of various chemical intermediates and may also serve as a fragrance or flavoring agent in certain applications. Its chemical behavior is influenced by the functional groups present, allowing it to participate in typical alcohol reactions, such as oxidation and esterification. Safety data indicates that, like many organic solvents, it should be handled with care, as it may pose health risks if inhaled or ingested.
Formula:C11H16O
InChI:InChI=1S/C11H16O/c1-2-6-11(12)9-10-7-4-3-5-8-10/h3-5,7-8,11-12H,2,6,9H2,1H3
InChI key:InChIKey=FCURFTSXOIATDW-UHFFFAOYSA-N
SMILES:C(C(CCC)O)C1=CC=CC=C1
Synonyms:- (±)-1-Phenyl-2-pentanol
- 1-Phenylpentan-2-Ol
- 2-Hydroxy-1-phenylpentane
- Alpha-Propylphenethyl Alcohol
- Benzeneethanol, α-propyl-
- Phenethyl alcohol, α-propyl-
- α-Propylbenzeneethanol
- α-Propylphenethyl alcohol
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Found 2 products.
2-Hydroxy-1-phenylpentane
CAS:Controlled Product<p>Applications 2-Hydroxy-1-phenylpentane is an impurity of Prolintane (P756100) synthesis.<br>References Hucker, H.B. et al.: Experientia, 28, 430 (1972); Hollister, L.E. et al.: J. Clin. Pharmacol. J. New Drugs, 10, 103 (1970); Kuitunen, T. et al.: Meth. Find. Exp. Clin. Pharmacol., 6, 265 (1984):<br></p>Formula:C11H16OColor and Shape:NeatMolecular weight:164.242-Hydroxy-1-phenylpentane
CAS:<p>2-Hydroxy-1-phenylpentane is a mandelonitrile with an alcohol group. It is a cytotoxic compound that can induce apoptosis in cancer cells. 2-Hydroxy-1-phenylpentane has been shown to inhibit the growth of MDA-MB-231 breast cancer cells and induce apoptosis. In addition, this compound also induces apoptosis in rat liver cells and human fibroblasts. This compound induces apoptosis by inhibiting the phosphatidylinositol 3 kinase (PI3K)/Akt pathways. 2-Hydroxy-1-phenylpentane also inhibits cell growth through a clonogenic assay in which it was found to be toxic to mouse embryonic stem cells at concentrations greater than or equal to 50 μM, but not at concentrations less than 10 μM. The toxicity of 2-Hydroxy-1-phenylpentane may be due to its ability to bind with DNA and</p>Formula:C11H16OPurity:Min. 95%Molecular weight:164.24 g/mol

