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3-PHENYL-1-PROPYNE

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3-PHENYL-1-PROPYNE Basic information

Product Name:
3-PHENYL-1-PROPYNE
Synonyms:
  • 3-PHENYL-1-PROPYNE
  • 3-PHENYL-1-PROPYNE 97%
  • 3-Phenyl-1-propyne, stabilized, 97%
  • 3-PHENYL-1-PROPYNE, 97%3-PHENYL-1-PROPYNE, 97%3-PHENYL-1-PROPYNE, 97%3-PHENYL-1-PROPYNE, 97%
  • Prop-2-yn-1-ylbenzene
  • (2-Propynyl)benzene
  • Propargylbenzene
  • 3-Phenyl-1-propyne,97%,stabilized
CAS:
10147-11-2
MF:
C9H8
MW:
116.16
Product Categories:
  • Alkynes
  • Organic Building Blocks
  • Terminal
Mol File:
10147-11-2.mol
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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.)
Flash point:
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
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Safety Information

Hazard Codes 
Xi
Risk Statements 
10-36/37/38
Safety Statements 
16-26-36/37/39-37/39
RIDADR 
UN 3295 3/PG 3
WGK Germany 
3
HazardClass 
3.2
PackingGroup 
III
HS Code 
29029090

MSDS

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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.

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