Basic information Safety Supplier Related

ETHYL-ALPHA-CYANO-4-HYDROXYCINNAMATE

Basic information Safety Supplier Related

ETHYL-ALPHA-CYANO-4-HYDROXYCINNAMATE Basic information

Product Name:
ETHYL-ALPHA-CYANO-4-HYDROXYCINNAMATE
Synonyms:
  • AKOS UB-20070
  • methyl (E)-2-cyano-3-(4-hydroxyphenyl)acrylate
  • ETHYL 2-CYANO-3-(4-HYDROXYPHENYL)ACRYLATE
  • ETHYL-ALPHA-CYANO-4-HYDROXYCINNAMATE
  • RARECHEM AK ML 0354
  • ethyl (2E)-2-cyano-3-(4-hydroxyphenyl)prop-2-enoate
  • Ethyl 2-cyano-3-(4-hydroxyphenyl)prop-2-enoate, 4-(2-Cyano-3-ethoxy-3-oxoprop-1-en-1-yl)phenol
  • (E)-Ethyl 2-cyano-3-(4-hydroxyphenyl)acrylate
CAS:
6935-44-0
MF:
C12H11NO3
MW:
217.22
Mol File:
6935-44-0.mol
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ETHYL-ALPHA-CYANO-4-HYDROXYCINNAMATE Chemical Properties

Melting point:
180-182°C
Boiling point:
381.8±32.0 °C(Predicted)
Density 
1.241±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
Solid
pka
7.42±0.15(Predicted)
Appearance
Light yellow to yellow Solid
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Safety Information

Hazard Codes 
Xi
HazardClass 
IRRITANT
HS Code 
2916120090
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ETHYL-ALPHA-CYANO-4-HYDROXYCINNAMATE Usage And Synthesis

Chemical Properties

Light-yellow crystalline powder

Synthesis

123-08-0

105-56-6

42205-38-9

GENERAL METHODS: 5 mmol of p-hydroxybenzaldehyde was added to a round-bottomed flask with 5 mmol of ethyl cyanoacetate, 25 mg of polymer-loaded catalyst (0.5 mol% substrate) and 5 mL of anhydrous ethanol, and the reaction was stirred at room temperature. The reaction process was monitored by silica gel thin layer chromatography (TLC) with hexane-ethyl acetate (10:1) as eluent. Upon completion of the reaction, the reaction mixture was filtered using filter paper and the catalyst on the filter paper was washed several times with ethanol. The washings and filtrates were combined and the product was isolated after concentration under reduced pressure. Typically, the products were of high purity and did not require further purification. All the products were reported in literature and characterized by melting point determination, Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance hydrogen spectroscopy (1H NMR).

References

[1] Tetrahedron Letters, 2014, vol. 55, # 15, p. 2352 - 2354
[2] Synlett, 2016, vol. 27, # 9, p. 1433 - 1437
[3] Tetrahedron, 2000, vol. 56, # 47, p. 9357 - 9364
[4] Synthetic Communications, 2003, vol. 33, # 5, p. 783 - 788
[5] Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 2010, vol. 49, # 3, p. 390 - 393

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