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| | 3-PHENYL-1-PROPYNE Basic information |
| | 3-PHENYL-1-PROPYNE Chemical Properties |
| Boiling point | 75 °C20 mm Hg(lit.) | | density | 0.934 g/mL at 25 °C(lit.) | | refractive index | n20/D 1.526(lit.) | | Fp | 126 °F | | storage temp. | Flammables area | | solubility | Chloroform (Sparingly), DMSO (Slightly) | | form | Liquid | | color | Clear colorless to yellow | | Specific Gravity | 0.934 | | Stability: | Volatile | | CAS DataBase Reference | 10147-11-2 |
| | 3-PHENYL-1-PROPYNE Usage And Synthesis |
| Chemical Properties | Clear colorless to yellow liquid | | Uses | 3-Phenyl-1-propyne is used as a starting material in the synthesis of 4-phenyl-2-butyn-1-ol. It is also used in the preparation of beta-hydroxytriazoles and indoles. | | Synthesis Reference(s) | The Journal of Organic Chemistry, 47, p. 1837, 1982 DOI: 10.1021/jo00349a007 | | General Description | 3-Phenyl-1-propyne is a 3-aryl-1-propyne. The electronic transition of the resonance-stabilized 1-phenylpropargyl radical, produced in a jet-cooled discharge of 3-phenyl-1-propyne, has been studied by laser-induced fluorescence excitation and dispersed single vibronic level fluorescence (SVLF) spectroscopy. The microwave rotational spectrum of 3-phenyl-1-propyne (propargyl benzene) has been studied and its stable conformation is reported to have coplanar carbon atoms. Reaction of N-methyl-N-phenylhydrazine or N-phenylhydrazine with 3-phenyl-1-propyne is reported to yield indoles. 3-Phenyl-1-propyne is reported to react with styrene oxide and sodium azide, to afford β-hydroxytriazoles. |
| | 3-PHENYL-1-PROPYNE Preparation Products And Raw materials |
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