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39244-10-5

39244-10-5 Structure

39244-10-5 Structure
IdentificationMore
[Name]

3-(3-FURYL)ACRYLIC ACID
[CAS]

39244-10-5
[Synonyms]

3-(3-FURYL)ACRYLIC ACID
RARECHEM BK HC S197
TIMTEC-BB SBB004191
TRANS-3-FURANACRYLIC ACID
Furan-3-acrylic acid
Furane-3-acrylicacid
3-Furanacrylic acid
[Molecular Formula]

C7H6O3
[MDL Number]

MFCD00075074
[Molecular Weight]

138.12
[MOL File]

39244-10-5.mol
Chemical PropertiesBack Directory
[Melting point ]

155-158 °C(lit.)
[Boiling point ]

261.4±15.0 °C(Predicted)
[density ]

1.280±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

Chloroform, Methanol
[form ]

Solid
[pka]

4.20±0.10(Predicted)
[color ]

Pale Yellow
[Water Solubility ]

Sparingly soluble in water (0.56 g/L at 25°C).
[BRN ]

1306450
[InChI]

InChI=1S/C7H6O3/c8-7(9)2-1-6-3-4-10-5-6/h1-5H,(H,8,9)
[InChIKey]

JHAPZUDWRRBZHZ-UHFFFAOYSA-N
[SMILES]

C(O)(=O)C=CC1C=COC=1
[CAS DataBase Reference]

39244-10-5(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S37/39:Wear suitable gloves and eye/face protection .
[WGK Germany ]

3
[HS Code ]

2932990090
Hazard InformationBack Directory
[Uses]

3-(3-Furyl)acrylic acid is used as an intermediate in chemical research and pharmaceuticals.
[Synthesis]

3-Furaldehyde

498-60-2

Malonic acid

141-82-2

3-(3-FURYL)ACRYLIC ACID

39244-10-5

To 12 mL of pyridine, 10.0 g of 3-furaldehyde and 15.0 g of malonic acid were added and heated with stirring at 80°C to 90°C for 2 hours. Upon completion of the reaction, the reaction solution was poured into ice water and the pH was adjusted to weakly acidic with 1 N hydrochloric acid. The precipitated crystals were collected by filtration, dissolved in ethyl acetate and the organic phase was washed with 1 N hydrochloric acid. The organic layer was dried with anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized by ethyl acetate-hexane mixed solvent to give 11.78 g (82% yield) of 3-(3-furyl)acrylic acid. The product was characterized by 1H-NMR (CDCl3): δ 7.70-7.67 (m, 2H), 7.45 (s, 1H), 6.62-6.61 (m, 1H), 6.16 (d, J = 15.8 Hz, 1H). Mass spectral analysis showed m/e: 138 (M+, base peak).

[References]

[1] Organic and Biomolecular Chemistry, 2010, vol. 8, # 24, p. 5483 - 5485
[2] ChemMedChem, 2018, vol. 13, # 18, p. 1972 - 1977
[3] Heterocycles, 1984, vol. 22, # 8, p. 1747 - 1757
[4] Patent: EP1724267, 2006, A1. Location in patent: Page/Page column 128
[5] Patent: WO2016/37578, 2016, A1. Location in patent: Page/Page column 111
Spectrum DetailBack Directory
[Spectrum Detail]

3-(3-FURYL)ACRYLIC ACID(39244-10-5)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

3-(3-Furyl)acrylic acid, 98%(39244-10-5)
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