Phenylpropiolaldehyde
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
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)
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
- F
- 9-19
- HS Code
- 29122990
MSDS
- Language:English Provider:3-Phenyl-2-propynal
- Language:English Provider:SigmaAldrich
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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Phenylpropiolaldehyde(2579-22-8)Related Product Information
- Phenylhydrazine
- 1H-Benzotriazole
- Salicylaldehyde
- Benproperine phosphate
- Cinnamaldehyde
- PHENYL VALERATE
- Paraldehyde
- Styrene-acrylic latex
- BENPROPERINE
- Phenylpropyl aldehyde
- 4-Morpholinopiperidine
- 4-PHENYL-3-BUTYN-2-ONE
- Phenylpropiolic acid
- METHYL PHENYLPROPIOLATE
- ETHYL PHENYLPROPIOLATE
- PHENYLPROPIOLALDEHYDE DIETHYL ACETAL
- (4-CHLORO-PHENYL)-PROPYNOIC ACID ETHYL ESTER
- NAPHTHALEN-1-YL-PROPYNOIC ACID