CAS 1123-85-9
:2-Phenyl-1-propanol
- (2R)-2-phenylpropan-1-ol
- (2S)-2-phenylpropan-1-ol
- (RS)-2-Phenyl-1-propanol
- (±)-2-Phenylpropanol
- (±)-β-Methylbenzeneethanol
- 1-Hydroxy-2-phenylpropane
- 1-Propanol, 2-phenyl-
- 2-Phenylpropan-1-Ol
- 2-Phenylpropyl alcohol
- 5,6,7,8-Tetrahydronaphthalen-2-Ol
- Benzeneethanol, β-methyl-
- Hydratropic alcohol
- Hydratropyl alcohol
- Hydratropyl alcohol~beta-Methylphenethyl alcohol
- NSC 5232
- Phenethyl alcohol, β-methyl-
- beta-Methylphenethyl alcohol
- β-Methylphenethyl alcohol
- See more synonyms
2-Phenyl-1-propanol
CAS:Formula:C9H12OPurity:>98.0%(GC)Color and Shape:Colorless to Almost colorless clear liquidMolecular weight:136.19(+/-)-2-Phenyl-1-propanol, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formula:C9H12OPurity:97%Color and Shape:Clear colorless, LiquidMolecular weight:136.192-Phenyl-1-propanol
CAS:2-Phenyl-1-propanol is a molecule with a hydroxyl group at the 2 position and a phenyl group at the 1 position. It is used as a film-forming polymer in coatings, adhesives, and elastomers. It is also used as an ingredient in glycol ethers, fatty acids, and enolate anions. 2-Phenyl-1-propanol has been shown to be synthesized by oxidative dehydrogenation of benzaldehyde and acetophenone. This reaction mechanism has been shown using chromatographic methods on two different solvents: one polar (water) and one nonpolar (tetrahydrofuran). The reaction proceeds with the formation of an enolate anion intermediate that reacts with water to form the alcohol product. The hydration process can be catalyzed by either sodium or potassium salts. The phase transition temperature for this compound is between -30°C and 60°
Formula:C9H12OPurity:Min. 95%Molecular weight:136.19 g/mol





