3-Furoic acid CAS 488-93-7

Introduction:Basic information about 3-Furoic acid CAS 488-93-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

3-Furoic acid Basic information

Product Name:3-Furoic acid
Synonyms:3-Furoic AcidSynonyMs 3-Furancarboxylic acid;3-Furancarboxylic acid (9CI);RARECHEM AL BO 1157;TIMTEC-BB SBB004325;3-FUROIC ACID;3-FURANCARBOXYLIC ACID;FURAN-3-CARBOXYLIC ACID;3-FUROIC ACID 99%
CAS:488-93-7
MF:C5H4O3
MW:112.08
EINECS:207-689-9
Product Categories:Building Blocks;C4 to C7;Chemical Synthesis;Heterocyclic Building Blocks;Furans;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Furan&Benzofuran
Mol File:488-93-7.mol

3-Furoic acid Chemical Properties

Melting point 120-122 °C (lit.)
Boiling point 229.64°C
density 1.3220
refractive index 1.4710 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka3.9(at 25℃)
form Solid
color Off-White to Beige
Water Solubility insoluble
BRN 108638
InChI1S/C5H4O3/c6-5(7)4-1-2-8-3-4/h1-3H,(H,6,7)
InChIKeyIHCCAYCGZOLTEU-UHFFFAOYSA-N
SMILESOC(=O)c1ccoc1
LogP1.030
CAS DataBase Reference488-93-7(CAS DataBase Reference)
NIST Chemistry Reference3-Furancarboxylic acid(488-93-7)

Safety Information

Hazard Codes Xi,C
Risk Statements 36/37/38-34
Safety Statements 26-36/37-45-36/37/39-36
WGK Germany 3
HazardClass IRRITANT
HS Code 29321900
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
Skin Irrit. 2

3-Furoic acid Usage And Synthesis

Description3-Furoic acid, also known as 3-carboxyfuran or 3-furoate, belongs to the class of organic compounds known as furoic acids. These are organic compounds containing a furoic acid moiety, with a structure characterized by a furan ring bearing a carboxylic acid group at the C2 or C3 carbon atom.
3-Furoic acid is an organic acid regularly occurring in urine of healthy individuals. It is used in synthesis of furan-2,5- and furan-2,4-dicarboxylic acid under solvent-free conditions via disproportionation reaction. It exhibits hypolipidemic activity in rodents. It lowers serum cholesterol and serum triglyceride levels in mice and rats.
Chemical Propertieswhite to light yellow crystal powde
Uses3-Furoic acid can be used as a reactant to synthesize:
Furan-2,5- and furan-2,4-dicarboxylic acid under solvent-free conditions via disproportionation reaction.
(±)-Hyperolactone A by reacting with 2-methylbutanal.
Furo[2,3-b]pyridin-4-one-5-carboxylate ester derivatives as potential non-nucleoside inhibitors of human herpesvirus polymerases.
Uses3-Furoic acid is used in synthesis of furan-2,5- and furan-2,4-dicarboxylic acid under solvent-free conditions via disproportionation reaction. It exhibits hypolipidemic activity in rodents. It lowers serum cholesterol and serum triglyceride levels in mice and rats.
Uses3-Furoic acid can be used as a reactant to synthesize:
  • Furan-2,5- and furan-2,4-dicarboxylic acid under solvent-free conditions via disproportionation reaction.
  • (±)-Hyperolactone A by reacting with 2-methylbutanal.
  • Furo[2,3-b]pyridin-4-one-5-carboxylate ester derivatives as potential non-nucleoside inhibitors of human herpesvirus polymerases.

DefinitionChEBI: A furoic acid carrying the carboxy group at position 3.
Synthesis Reference(s)Tetrahedron Letters, 26, p. 1509, 1985 DOI: 10.1016/S0040-4039(00)98538-1
Biological Activity3-Furoic acid exhibits hypolipidemic activity in rodents. It lowers serum cholesterol and serum triglyceride levels in mice and rats.
Biochem/physiol Actions3-Furoic acid exhibits hypolipidemic activity in rodents. It lowers serum cholesterol and serum triglyceride levels in mice and rats.
Purification MethodsCrystallise the acid from water or aqueous EtOH, and sublime it in a vacuum. [Beilstein 18 I 439, 18 III/IV 4052, 18/6 V 196.]

3-Furoic acid Preparation Products And Raw materials

Raw materialsHydrogen bromide-->Sodium ethoxide
Preparation ProductsTETRAHYDRO-3-FUROIC ACID-->3-FURYLMETHYLAMINE-->3-(Chloromethyl)furan-->Telatinib-->Carbamic acid, 3-furanyl-, 1,1-dimethylethyl ester (9CI)-->TETRAHYDRO-FURAN-3-CARBONYL CHLORIDE-->2-Methyl-3-furoic Acid-d3-->3-Furancarboxylic acid, 5-acetyl--->ETHYL 6H-FURO[2,3-B]PYRROLE-5-CARBOXYLATE-->2-iodofuran-3-carboxylic acid-->1H-Benzimidazole,2-(3-furanyl)-(9CI)-->2-Bromo-3-furoyl chloride
3-Furanmethanol, tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-, (2
3''-HABA KanaMycin A CAS 50725-25-2
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