2-Furancarboxylic Acid

• CAS: 88-14-2
• Catalog Number: ACM88142
• Category: Furans
• Molecular Weight: 112.08
• Molecular Formula: C5H4O3
• Synonyms: 2-Furoic Acid, Pyromucic Acid
• Melting Point: 130.0-133.0 °C(lit.)

Custom Q&A

What is the molecular formula of 2-Furancarboxylic Acid?

The molecular formula of 2-Furancarboxylic Acid is C5H4O3.

What is the molecular weight of 2-Furancarboxylic Acid?

The molecular weight of 2-Furancarboxylic Acid is 112.08 g/mol.

What is the IUPAC name of 2-Furancarboxylic Acid?

The IUPAC name of 2-Furancarboxylic Acid is furan-2-carboxylic acid.

What is the InChI of 2-Furancarboxylic Acid?

The InChI of 2-Furancarboxylic Acid is InChI=1S/C5H4O3/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7).

What is the InChIKey of 2-Furancarboxylic Acid?

The InChIKey of 2-Furancarboxylic Acid is SMNDYUVBFMFKNZ-UHFFFAOYSA-N.

What is the CAS number of 2-Furancarboxylic Acid?

The CAS number of 2-Furancarboxylic Acid is 88-14-2.

What is the European Community (EC) number of 2-Furancarboxylic Acid?

The European Community (EC) number of 2-Furancarboxylic Acid is 201-803-0.

What is the molecular weight of 2-Furancarboxylic Acid according to PubChem?

The molecular weight of 2-Furancarboxylic Acid is 112.08 g/mol according to PubChem.

How many hydrogen bond donor counts does 2-Furancarboxylic Acid have?

2-Furancarboxylic Acid has 1 hydrogen bond donor count.

How many hydrogen bond acceptor counts does 2-Furancarboxylic Acid have?

2-Furancarboxylic Acid has 3 hydrogen bond acceptor counts.

Synthetic Use

Upstream Synthesis Route 1

• 2280-44-6
• 657-27-2

• 88-14-2
• 6338-41-6
• 34371-14-7

Reference: [1] Acta Chemica Scandinavica, Series B: Organic Chemistry and Biochemistry, 1984, vol. 38, # 8, p. 689 - 694

Upstream Synthesis Route 2

• 6728-26-3
• 1129294-89-8

• 98-01-1
• 496-64-0
• 88-14-2
• 13419-69-7
• 1401094-48-1
• 1401094-49-2
• 1309945-34-3

Reference: [1] Journal of Agricultural and Food Chemistry, 2012, vol. 60, # 40, p. 9967 - 9973,7

Downstream Synthesis Route 1

• 88-14-2

• 4412-91-3

Reference: [1] Beilstein Journal of Organic Chemistry, 2013, vol. 9, p. 2925 - 2933

Downstream Synthesis Route 2

• 88-14-2
• 64-17-5

• 16874-34-3

Reference: [1]Patent: US2843607,1954,

Downstream Synthesis Route 3

• 88-14-2
• 75-07-0

• 16874-34-3

Reference: [1]Patent: US2843607,1954,

Downstream Synthesis Route 4

• 88-14-2
• 100-66-3

• 36112-61-5

Reference: [1]Journal of the American Chemical Society,1941,vol. 63,p. 1857,1859
[2]Bulletin of the Chemical Society of Japan,1975,vol. 48,p. 3356 - 3366
[3]Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry,1982,vol. 21,p. 192 - 196
[4]Patent: CN108863775,2018,A .Location in patent: Paragraph 0035; 0037; 0038-0039; 0041; 0043; 0045; 0047

* For details of the synthesis route, please refer to the original source to ensure accuracy.