Tetrahydrofuran-2-Carboxylic Acid

• CAS: 16874-33-2
• Catalog Number: ACM16874332
• Category: Furans
• Molecular Weight: 116.12
• Molecular Formula: C5H8O3
• Synonyms: 2-Tetrahydrofuroic Acid
• Boiling Point: 243.2 °C at 760 mmHg
• Flash Point: 139°C(lit.)
• Density: 1.1700 g/mL at 25 °C(lit.)
• Appearance: Colorless to yellow viscous liquid

Custom Q&A

What is the molecular formula of Tetrahydrofuran-2-carboxylic Acid?

The molecular formula of Tetrahydrofuran-2-carboxylic Acid is C5H8O3.

What is the molecular weight of Tetrahydrofuran-2-carboxylic Acid?

The molecular weight of Tetrahydrofuran-2-carboxylic Acid is 116.11 g/mol.

What is the IUPAC name of Tetrahydrofuran-2-carboxylic Acid?

The IUPAC name of Tetrahydrofuran-2-carboxylic Acid is oxolane-2-carboxylic acid.

What is the InChI of Tetrahydrofuran-2-carboxylic Acid?

The InChI of Tetrahydrofuran-2-carboxylic Acid is InChI=1S/C5H8O3/c6-5(7)4-2-1-3-8-4/h4H,1-3H2,(H,6,7).

What is the InChIKey of Tetrahydrofuran-2-carboxylic Acid?

The InChIKey of Tetrahydrofuran-2-carboxylic Acid is UJJLJRQIPMGXEZ-UHFFFAOYSA-N.

What is the Canonical SMILES of Tetrahydrofuran-2-carboxylic Acid?

The Canonical SMILES of Tetrahydrofuran-2-carboxylic Acid is C1CC(OC1)C(=O)O.

What is the CAS number of Tetrahydrofuran-2-carboxylic Acid?

The CAS number of Tetrahydrofuran-2-carboxylic Acid is 16874-33-2.

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

The European Community (EC) number of Tetrahydrofuran-2-carboxylic Acid is 605-530-1.

What is the Wikidata ID of Tetrahydrofuran-2-carboxylic Acid?

The Wikidata ID of Tetrahydrofuran-2-carboxylic Acid is Q15634146.

What is the Wikipedia page for Tetrahydrofuran-2-carboxylic Acid?

The Wikipedia page for Tetrahydrofuran-2-carboxylic Acid is "Tetrahydro-2-furoic_acid".

Synthetic Use

Upstream Synthesis Route 1

• 97-99-4

• 16874-33-2

Reference: [1] Journal of Organic Chemistry, 1980, vol. 45, # 1, p. 48 - 61
[2] Journal of the American Chemical Society, 2016, vol. 138, # 27, p. 8344 - 8347
[3] Journal of Medicinal Chemistry, 1995, vol. 38, # 15, p. 2830 - 2841

Upstream Synthesis Route 2

• 88-14-2

• 16874-33-2

Reference: [1] Monatshefte fur Chemie, 2000, vol. 131, # 12, p. 1335 - 1343

Upstream Synthesis Route 3

• 542-28-9

• 16874-33-2

Reference: [1] Journal of the American Chemical Society, 2001, vol. 123, # 33, p. 8149 - 8150

Downstream Synthesis Route 1

• 16874-33-2

• 52449-98-6

Reference: [1]Patent: WO2010/135504,2010,A1 .Location in patent: Page/Page column 75-76

Downstream Synthesis Route 2

• 16874-33-2

• 87392-07-2

Reference: [1]Patent: CN109705064,2019,A .Location in patent: Paragraph 0020; 0022; 0023; 0024; 0025; 0036

Downstream Synthesis Route 3

• 16874-33-2
• 67-56-1

• 37443-42-8

Reference: [1]Tetrahedron,2006,vol. 62,p. 422 - 433

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