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4-ETHYNYLBENZALDEHYDE

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4-ETHYNYLBENZALDEHYDE Basic information

Product Name:
4-ETHYNYLBENZALDEHYDE
Synonyms:
  • 4-ethynylbezaldehyde
  • 4-ETHYNYLBENZALDEHYDE,95%
  • CHEMBRDG-BB 4003406
  • 4-ETHYNYLBENZALDEHYDE
  • Benzaldehyde, 4-ethynyl- (9CI)
  • Benzaldehyde,4-ethynyl-
  • 4-Ethynylbenzaldehyde 97%
  • Zinc02548316
CAS:
63697-96-1
MF:
C9H6O
MW:
130.14
Product Categories:
  • Aldehydes
  • C9
  • Carbonyl Compounds
  • ALDEHYDE
Mol File:
63697-96-1.mol
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4-ETHYNYLBENZALDEHYDE Chemical Properties

Melting point:
89-93 °C (lit.)
Boiling point:
223.8±23.0 °C(Predicted)
Density 
1.07±0.1 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Store in freezer, under -20°C
form 
Powder or Crystalline Powder
color 
White to orange to brown
λmax
297nm(CH3CN)(lit.)
InChI
InChI=1S/C9H6O/c1-2-8-3-5-9(7-10)6-4-8/h1,3-7H
InChIKey
BGMHQBQFJYJLBP-UHFFFAOYSA-N
SMILES
C(=O)C1=CC=C(C#C)C=C1
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-26-36
WGK Germany 
3
HS Code 
29122990

MSDS

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4-ETHYNYLBENZALDEHYDE Usage And Synthesis

Uses

4-?Ethynylbenzaldehyde is commonly used in solar cells as the acceptor unit.

Synthesis Reference(s)

The Journal of Organic Chemistry, 46, p. 2280, 1981 DOI: 10.1021/jo00324a015

Synthesis

77123-57-0

63697-96-1

General procedure for the synthesis of 4-ethynylbenzaldehyde from 4-trimethylsilylethynylbenzaldehyde: Compound 4 (727 mg, 3.6 mmol) was dissolved in 15 mL of anhydrous THF, followed by the addition of 2 mL of aqueous KOH (298 mg, 4 mmol). The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the THF solvent was removed by rotary evaporator. The reaction mixture was extracted with ethyl acetate (EA) and washed three times with saturated NaCl solution. The combined organic phases were dried with anhydrous Na2SO4, filtered and concentrated. Finally, purification by column chromatography (eluent was petroleum ether and dichloromethane, 1:1, v/v) gave 450 mg of compound 5 as a light yellow solid in 97% yield.

References

[1] Journal of the American Chemical Society, 2009, vol. 131, # 2, p. 634 - 643
[2] Chemical Communications, 2011, vol. 47, # 4, p. 1282 - 1284
[3] Journal of Materials Chemistry A, 2013, vol. 1, # 34, p. 10008 - 10015
[4] ChemPhysChem, 2016, p. 2066 - 2078
[5] Journal of the American Chemical Society, 2016, vol. 138, # 51, p. 16703 - 16710

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