PHENYLPROPIOLALDEHYDE DIETHYL ACETAL
PHENYLPROPIOLALDEHYDE DIETHYL ACETAL Basic information
- Product Name:
- PHENYLPROPIOLALDEHYDE DIETHYL ACETAL
- Synonyms:
-
- (3,3-Diethoxy-1-propynyl)benzene
- 3-Phenylpropynal diethyl acetal
- Propiolaldehyde, phenyl-, diethyl acetal
- PHENYLPROPIOLALDEHYDE DIETHYL ACETAL
- PHENYLPROPIOLIC ALDEHYDE DIETHYLACETAL
- PHENYLPROPARGYL ALDEHYDE DIETHYL ACETAL
- 3-PHENYL-2-PROPYNYL ALDEHYDE DIETHYL ACETAL
- (3,3-DIETHOXYPROP-1-YN-1-YL)BENZENE
- CAS:
- 6142-95-6
- MF:
- C13H16O2
- MW:
- 204.26
- EINECS:
- 228-143-6
- Product Categories:
-
- Acetals/Ketals/Ortho Esters
- Building Blocks
- Chemical Synthesis
- Organic Building Blocks
- Oxygen Compounds
- Mol File:
- 6142-95-6.mol
PHENYLPROPIOLALDEHYDE DIETHYL ACETAL Chemical Properties
- Boiling point:
- 99-100 °C2 mm Hg(lit.)
- Density
- 0.991 g/mL at 25 °C(lit.)
- refractive index
- n20/D 1.517(lit.)
- Flash point:
- >230 °F
- storage temp.
- Sealed in dry,2-8°C
- BRN
- 2049715
- CAS DataBase Reference
- 6142-95-6(CAS DataBase Reference)
Safety Information
- Safety Statements
- 24/25
- WGK Germany
- 3
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
PHENYLPROPIOLALDEHYDE DIETHYL ACETAL Usage And Synthesis
Chemical Properties
CLEAR COLOURLESS TO YELLOW LIQUID
Preparation
To a flask equipped with a 12-in. Vigreux column and distillation head is added 74.0 gm (0.50 mole) of triethyl orthoformate, 51.0 gm (0.50 mole)of phenylacetylene, and 3.0 gm of zinc iodide* catalyst. The flask must first be heated to 135°C before ethanol starts to reflux. The ethanol distillate (26.4 gm) boiling at 65°-88°C is removed over a period of 1 hr while the temperature of the reaction mixture is raised to 200°-210°C. The reaction mixture is cooled and filtered, the precipitate washed with 5 ml of ether and the ether combined with the filtrate is distilled to afford 73-80 gm (72-78%), b.p. 99-100°C (2.0 mm Hg). The IR spectrum showed absorption at 4.5-μ (—C=C—) and 9.0-μ region ( - C — O ).
Synthesis Reference(s)
The Journal of Organic Chemistry, 49, p. 2031, 1984 DOI: 10.1021/jo00185a045
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