Basic information Safety Supplier Related

PHENYLPROPIOLALDEHYDE DIETHYL ACETAL

Basic information Safety Supplier Related

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
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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)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3

MSDS

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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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