3-(2-Furyl)acrylic acid
3-(2-Furyl)acrylic acid
  • CAS No.:539-47-9
Other grades of this product :
3-(2-Furyl)acrylic acid Basic information
Product Name:3-(2-Furyl)acrylic acid
Synonyms:(2E)-3-(2-Furyl)-2-propenoic acid;(2-Furyl)acrylic acid;3-(2-Furanyl)-2-propenoic acid;3-(2-furanyl)-2-propenoicaci;2-PROPENOIC ACID, 3-(2-FURANYL)-;3-(2-FURYL)ACRYLIC ACID;3-(2-furyl)-2-propenoic acid;FURYLACRYLIC ACID
CAS:539-47-9
MF:C7H6O3
MW:138.12
EINECS:208-718-8
Product Categories:Building Blocks;C4 to C7;Furan&Benzofuran;Heterocycles;Chemical Synthesis;Heterocyclic Building Blocks;Pharmaceutical Intermediates;Aromatic Cinnamic Acids, Esters and Derivatives;Organic acids;Heterocyclic Compounds;Furans
Mol File:539-47-9.mol
3-(2-Furyl)acrylic acid Chemical Properties
Melting point 139-141 °C (lit.)
Boiling point 286 °C (lit.)
density 1.2667 (rough estimate)
refractive index 1.4600 (estimate)
Fp 286°C
storage temp. Store below +30°C.
solubility Soluble in dichloromethane and diethyl ether.
pka4.39±0.10(Predicted)
form Solid
color Pale Beige
Water Solubility 2g/L(20 ºC)
Merck 14,4297
BRN 81046
Stability:Light Sensitive
CAS DataBase Reference539-47-9(CAS DataBase Reference)
NIST Chemistry Reference2-Propenoic acid, 3-(2-furanyl)-(539-47-9)
EPA Substance Registry System2-Propenoic acid, 3-(2-furanyl)- (539-47-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 22-24/25
WGK Germany 3
RTECS LT8560000
TSCA Yes
HazardClass IRRITANT
HS Code 29321900
MSDS Information
ProviderLanguage
3-(2-Furyl)-2-propenoic acid English
SigmaAldrich English
ACROS English
ALFA English
3-(2-Furyl)acrylic acid Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
Uses3-(2-Furyl)acrylic acid is derivatives used in perfumes.
Uses3-(2-Furyl)acrylic acid is a reactant used in the preparation of heteroaryl-substituted bis-trifluoromethyl carbinols and trifluoroacetophenone derivatives malonyl-CoA decarboxylase (MCD) inhibitors.
Synthesis Reference(s)Journal of the American Chemical Society, 78, p. 3425, 1956 DOI: 10.1021/ja01595a044Organic Syntheses, Coll. Vol. 3, p. 426, 1955
Purification MethodsCrystallise the cis-isomer from *C6H6 and the trans-isomer from H2O, *C6H6 or pet ether (b 80-100o)(charcoal). [Beilstein 18 H 301, 18 III/IV 4143, 18/6 V 306.]

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