CAS 14903-90-3

3-Bromo-2-furoic acid

Description:

3-Bromo-2-furoic acid is an organic compound characterized by its furan ring structure, which is a five-membered aromatic ring containing one oxygen atom. The presence of a bromine atom at the 3-position and a carboxylic acid group at the 2-position contributes to its unique chemical properties. This compound is typically a white to off-white solid and is soluble in polar solvents due to the carboxylic acid functionality. It exhibits acidic behavior, capable of donating a proton in solution, which is characteristic of carboxylic acids. The bromine substituent can influence the compound's reactivity, making it useful in various chemical synthesis applications, including the development of pharmaceuticals and agrochemicals. Additionally, 3-bromo-2-furoic acid can participate in electrophilic aromatic substitution reactions and can serve as a building block for more complex organic molecules. Its specific applications and reactivity may vary based on the conditions and the presence of other functional groups in a reaction.

Formula: C₅H₃BrO₃

InChI: InChI=1/C5H3BrO3/c6-3-1-2-9-4(3)5(7)8/h1-2H,(H,7,8)

SMILES: c1coc(c1Br)C(=O)O

Synonyms:

• 2-Furancarboxylic Acid, 3-Bromo-
• 3-Bromofuran-2-Carboxylic Acid

2-Furancarboxylic acid, 3-bromo-

CAS: 14903-90-3

Formula: C₅H₃BrO₃

Purity: 96%

Color and Shape: Solid

Molecular weight: 190.9795

Ref: IN-DA001LD0

3-bromofuran-2-carboxylic acid

CAS: 14903-90-3

3-bromofuran-2-carboxylic acid

Purity: 95%

Molecular weight: 190.98g/mol

Ref: 54-OR907958

3-Bromofuran-2-carboxylic acid

CAS: 14903-90-3

Formula: C₅H₃BrO₃

Purity: 96%

Color and Shape: No data available.

Molecular weight: 190.98

Ref: 10-F238905

3-Bromo-2-furoic Acid

CAS: 14903-90-3

3-Bromo-2-furoic acid is an intermediate in the synthesis of 3,4-dihydro-2H-pyran. It is produced by the oxidation of 2-furoic acid and can be synthesized by the reaction of furyl with biphenyl. 3-Bromo-2-furoic acid is a competitive inhibitor of glutamate dehydrogenase and glutamate synthetase. Inhibition of these enzymes prevents the conversion of glutamate to glutamine, which leads to elevated levels of glutamate in the brain, resulting in neurotoxicity. 3-Bromo-2-furoic acid also inhibits nicotinic acetylcholine receptors at low concentrations and has been shown to inhibit mitochondrial respiration. This drug has been used to treat hypertension in rats.

Formula: C₅H₃BrO₃

Purity: Min. 95%

Molecular weight: 190.98 g/mol

Ref: 3D-PAA90390