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10147-11-2

  • Product Name:3-PHENYL-1-PROPYNE
  • Molecular Formula:C9H8
  • Molecular Weight:116.163
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Product Details

Purity:99%

Manufacturer Supply Best Quality 3-PHENYL-1-PROPYNE 10147-11-2 with Efficient Transportation

  • Molecular Formula:C9H8
  • Molecular Weight:116.163
  • Vapor Pressure:1.2mmHg at 25°C 
  • Refractive Index:n20/D 1.526(lit.) 
  • Boiling Point:75 °C20 mm Hg(lit.)  
  • Flash Point:126 °F  
  • PSA：0.00000 
  • Density:0.934 g/mL at 25 °C(lit.)  
  • LogP:1.86230 

3-PHENYL-1-PROPYNE(Cas 10147-11-2) Usage

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.

InChI:InChI=1/C9H8/c1-2-6-9-7-4-3-5-8-9/h1,3-5,7-8H,6H2

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10147-11-2 Process route

benzoylpyrazole
10199-66-3

benzoylpyrazole

1-Phenylprop-1-yne
673-32-5

1-Phenylprop-1-yne

2-phenylfuran
17113-33-6

2-phenylfuran

1-phenylpropadiene
2327-99-3

1-phenylpropadiene

propargyl benzene
10147-11-2

propargyl benzene

phenylacetylene
536-74-3

phenylacetylene

1-indene
95-13-6

1-indene

Conditions
Conditions Yield
at 900 ℃; flash-vacuum pyrolysis under low pressure;
56%
1-(trimethylsilyl)-3-phenylprop-1-yne
31683-47-3

1-(trimethylsilyl)-3-phenylprop-1-yne

propargyl benzene
10147-11-2

propargyl benzene

Conditions
Conditions Yield
With potassium carbonate; In methanol; at 0 ℃;
93.5%
With potassium carbonate; In methanol; water; at 0 - 20 ℃; for 2h;
With potassium carbonate; In methanol; at 20 ℃; for 2h; Cooling with ice;
5 g
With trimethylsilyl trifluoromethanesulfonate; water; In dichloromethane; at 20 ℃; for 2h;

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