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Thermo Scientific Chemicals
3-Furoic acid, 99%
CAS: 488-93-7 | C5H4O3 | 112.08 g/mol
化学物質識別子
CAS488-93-7
IUPAC Namefuran-3-carboxylic acid
Molecular FormulaC5H4O3
InChI KeyIHCCAYCGZOLTEU-UHFFFAOYSA-N
SMILESOC(=O)C1=COC=C1
さらに表示
仕様
スペックシート
スペックシートAppearance (Color)White to pale brown
Assay (Silylated GC)>98.5%
Formcrystals or crystalline powder
Assay (Aqueous acid-base Titration)>98.5%
Solution Test1%w/w in ethanol will be cl1% w/v in ethanol: clear to very faintly turbid by JIS K8001
3-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.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
3-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.
Solubility
Soluble in water, ether, alcohol, ethanol, and methanol.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
3-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.
Solubility
Soluble in water, ether, alcohol, ethanol, and methanol.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Takamasa Kinoshita.; Kouichi Miyano.; Toshio Miwa. The Birch Reduction of Heterocyclic Carboxylic Acids. I. The Birch Reduction of 3-Furoic Acid. Bulletin of the Chemical Society of Japan. 1975, 48 (6), 1865-18677.
- Antonio J. Moreno-Vargas.; Inmaculada Robina.; Raynald Demange.; Pierre Vogel. Synthesis and Glycosidase Inhibitory Activities of 5-(1',4'-Dideoxy-1',4'-imino-D-erythrosyl)-2-methyl-3-furoic Acid (=5-[(3S,4R)-3,4-Dihydroxypyrrolidin-2-yl]-2-methylfuran-3-carboxylic Acid) Derivatives: New Leads as Selective α-L-Fucosidase and β-Galactosidase Inhibitors. Helvetica Chimica Acta. 2013, 86 (6), 1894-1913.