Misplaced Pages

Propiolaldehyde

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
(Redirected from Propynal)
Propiolaldehyde
Names
Preferred IUPAC name Prop-2-ynal
Other names Propynal; Propiolic aldehyde
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.009.871 Edit this at Wikidata
PubChem CID
UNII
CompTox Dashboard (EPA)
SMILES
  • C#CC=O
Properties
Chemical formula C3H2O
Molar mass 54.048 g·mol
Appearance colorless liquid
Density 0.9152 g/cm
Boiling point 54–57 °C (129–135 °F; 327–330 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Infobox references
Chemical compound

Propiolaldehyde is an organic compound with molecular formula HC2CHO. It is the simplest chemical compound containing both alkyne and aldehyde functional groups. It is a colorless liquid with explosive properties.

Reactions

The compound exhibits reactions expected for an electrophilic alkynyl aldehyde. It is a dienophile and a good Michael acceptor. Grignard reagents add to the carbonyl center. Its explosive properties are attributed to the exothermicity of its polymerization.

Preparation

Its acetal can be prepared from acrolein.

Occurrence in interstellar medium

Propynal has been observed in the interstellar medium. It is hypothesized to be formed from a carbon monoxide-acetylene complex. Another possible pathway is through the reaction of propynylidyne (C3H) with water.

Hazards

The compound is explosive, possibly because it tends to polymerize.

See also

References

  1. ^ P. Perlmutter (2001). "Propargyl Aldehyde". Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rp262m. ISBN 978-0471936237.
  2. A. Le Coq and A. Gorgues (1979). "Alkyness via Phase Transfer-Catalyzed Dehydrohalogenatiion: Propiolaldehyde Diethyl Acetal". Organic Syntheses. 59: 10. doi:10.15227/orgsyn.059.0010.
  3. Zhou, Li; Ralf I. Kaiser (2008), "Pathways to Oxygen-Bearing Molecules in the Interstellar Medium and in Planetary Atmospheres: Cyclopropenone (c-C3H2O) and Propynal (HCCCHO)", The Astrophysical Journal, 686 (2): 1493–1502, doi:10.1086/591072
  4. Xie, Hong-bin; Chang-bin Shao (2007), "Radical-Molecule Reaction C3H + H2O on Amorphous Water Ice: A Promising Route for Interstellar Propynal", The Astrophysical Journal, 670 (1): 449–456, doi:10.1086/520757
Molecules detected in outer space
Molecules
Diatomic







Triatomic
Four
atoms
Five
atoms
Six
atoms
Seven
atoms
Eight
atoms
Nine
atoms
Ten
atoms
or more
Deuterated
molecules
Unconfirmed
Related
Categories: