488-93-7 | Furan-3-carboxylic acid

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$10.00	$7.00
5g	98%	in stock	$12.00	$8.00
10g	98%	in stock	$20.00	$14.00
25g	98%	in stock	$28.00	$19.00

Description

• Catalog Number: AB44585
• Chemical Name: Furan-3-carboxylic acid
• CAS Number: 488-93-7
• Molecular Formula: C5H4O3
• Molecular Weight: 112.0835
• MDL Number: MFCD00005350
• SMILES: OC(=O)c1cocc1
• NSC Number: 349941

Computed Properties

• Complexity: 99.8
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1

Upstream Synthesis Route

3-Furoic Acid, also known as furan-3-carboxylic acid, is a versatile compound widely utilized in chemical synthesis for its unique reactivity and properties. In organic chemistry, 3-Furoic Acid serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals due to its ability to undergo a range of chemical transformations.One of the key applications of 3-Furoic Acid in chemical synthesis is as a precursor for the synthesis of heterocyclic compounds. By utilizing the carboxylic acid group and the furan ring structure, chemists can easily introduce functional groups and modify the molecular structure to generate diverse heterocycles with specific properties. These heterocyclic compounds exhibit a wide range of biological activities and are of interest in drug discovery and development.Furthermore, 3-Furoic Acid can be employed as a starting material for the synthesis of various aromatic compounds. Through functional group interconversions and substitution reactions, chemists can access a broad spectrum of aromatic derivatives for use in industries such as flavors and fragrances, dyes, and materials science.Additionally, 3-Furoic Acid is utilized in the preparation of polymer materials, where its reactivity allows for the incorporation of furan moieties into the polymer backbone, imparting desirable properties such as thermal stability, biodegradability, and high performance.Overall, the versatile nature of 3-Furoic Acid makes it a valuable tool in chemical synthesis, enabling the generation of diverse compounds with wide-ranging applications in pharmaceuticals, materials science, and other fields.

Literature

• Micellar electrokinetic chromatography method for the simultaneous determination of furanic compounds in honey and vegetable oils.

  Talanta 20120815

• Enantioselective synthesis of (-)-paeonilide.

  Chemical communications (Cambridge, England) 20120407

• Kinase inhibitors from marine sponges.

  Marine drugs 20110101

• A direct RP-HPLC method for the determination of furanic aldehydes and acids in honey.

  Talanta 20090415

• Regioselective palladium-catalyzed arylation of 3-carboalkoxy furan and thiophene.

  Organic letters 20030206