Skip to Content
Merck
All Photos(3)

Documents

F20505

Sigma-Aldrich

2-Furoic acid

98%

Synonym(s):

Furan-2-carboxylic acid

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C5H4O3
CAS Number:
88-14-2
Molecular Weight:
112.08
Beilstein:
110149
EC Number:
201-803-0
MDL number:
MFCD00003238
UNSPSC Code:
12352100
PubChem Substance ID:
24894811
NACRES:
NA.22

Assay

98%

bp

230-232 °C (lit.)

mp

128-132 °C (lit.)

SMILES string

OC(=O)c1ccco1

InChI

1S/C5H4O3/c6-5(7)4-2-1-3-8-4/h1-3H,(H,6,7)

InChI key

SMNDYUVBFMFKNZ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Some of the applications of 2-furoic acid include:
  • Synthesis of a single-molecule magnet, Mn11Gd2 based high-nuclearity heterometallic complex.
  • Synthesis of orally active antidiabetic vanadyl complex, bis(α-furancarboxylato)oxovanadium(IV).
  • As a ligand in the synthesis of luminescent 4f-3d heterometallic one-dimensional coordination polymers.
  • Synthesis of biocompatible multifunctional dextran furoate nanospheres.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

282.7 °F - closed cup

Flash Point(C)

139.3 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

Ethyl 2-furoate ≥98%, FG

Sigma-Aldrich

W501301

Ethyl 2-furoate

3-(2-Furyl)propionic acid 97%

Sigma-Aldrich

667730

3-(2-Furyl)propionic acid

Syntheses, crystal structure and luminescence property of novel 4f-3d heterometallic one-dimensional coordination polymers.
Yin M.
Journal of Physics and Chemistry of Solids, 67(7), 1372-1378 (2006)
Structure Design of Multifunctional Furoate and Pyroglutamate Esters of Dextran by Polymer?Analogous Reactions.
Hornig S.
Macromolecular Bioscience, 7(3), 297-306 (2007)
Jin-Xin Gao et al.
Phytopathology, 104(4), 332-339 (2013-10-19)
The maize pathotype Cochliobolus lunatus causes Curvularia leaf spot by producing a non-host-specific toxin known as methyl 5-(hydroxymethyl) furan-2-carboxylate (M5HF2C). However, related research that explores the genes that control the production of this toxin is rare. In the current work
A bell-shaped Mn11Gd2 single-molecule magnet.
Mereacre VM.
Journal of the American Chemical Society, 129(30), 9248-9249 (2007)
A new orally active antidiabetic vanadyl complex-bis (α-furancarboxylato) oxovanadium (IV).
Xie M.
Journal of Inorganic Biochemistry, 99(2), 546-551 (2005)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service