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Phenylpropiolaldehyde

Basic information Uses Safety Supplier Related

Phenylpropiolaldehyde Basic information

Product Name:
Phenylpropiolaldehyde
Synonyms:
  • 2-Propynal, 3-phenyl-
  • 3-Phenylpropynal
  • Benzenepropiolaldehyde
  • Phenylacetylenecarboxaldehyde
  • Phenylpropynal
  • Propiolaldehyde, phenyl-
  • PHENYLPROPARGYL ALDEHYDE
  • PHENYLPROPIOLALDEHYDE
CAS:
2579-22-8
MF:
C9H6O
MW:
130.14
EINECS:
219-942-0
Product Categories:
  • Aldehydes
  • Building Blocks
  • C9
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
Mol File:
2579-22-8.mol
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Phenylpropiolaldehyde Chemical Properties

Melting point:
139-140 °C (decomp)
Boiling point:
118 °C13 mm Hg(lit.)
Density 
1.064 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.604(lit.)
Flash point:
202 °F
storage temp. 
2-8°C
form 
liquid
color 
Clear, dark red/orange
BRN 
1099281
InChI
InChI=1S/C9H6O/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6,8H
InChIKey
IDASOVSVRKONFS-UHFFFAOYSA-N
SMILES
C(=O)C#CC1=CC=CC=C1
CAS DataBase Reference
2579-22-8(CAS DataBase Reference)
NIST Chemistry Reference
Phenylpropargyl aldehyde(2579-22-8)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-36-22
Safety Statements 
26-36
RIDADR 
UN 2810 6.1/PG 3
WGK Germany 
3
9-19
HS Code 
29122990

MSDS

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Phenylpropiolaldehyde Usage And Synthesis

Uses

Due to its diverse reactivity, phenylpropyne aldehyde is frequently used in organic chemistry research to explore new reaction pathways and develop novel synthetic methods. Its unique structure and varied reactivity make it an important synthetic intermediate in synthetic chemistry; for example, the reaction of phenylpropyne aldehyde with Wittig reagents can produce conjugated enyne compounds, which have potential applications in optoelectronics and organic electronic materials.

Chemical Properties

Phenylpropiolaldehyde is a dark red or orange liquid at room temperature and pressure, and is sensitive to oxidants. It is an unsaturated aldehyde compound, which contains a carbon-carbon triple bond structure and an aldehyde unit in its structure, and has a variety of chemical reaction pathways. This compound can undergo a nucleophilic addition reaction with a Grignard reagent to obtain propargyl alcohol derivatives

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