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F20505

2-Furoic acid

Name: 2-Furoic acid
Brand: ALDRICH

98%

Synonym(s):

Furan-2-carboxylic acid

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About This Item

Empirical Formula (Hill Notation):

C₅H₄O₃

CAS Number:

88-14-2

Molecular Weight:

112.08

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24894811

EC Number:

201-803-0

Beilstein/REAXYS Number:

110149

MDL number:

MFCD00003238

Assay:

98%

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Properties

Quality Level

100

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

Description

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.

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pictograms

GHS05

signalword

Danger

hcodes

H314

pcodes

P260 - P280 - P303 + P361 + P353 - P304 + P340 + P310 - P305 + P351 + P338 - P363

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

flash_point_f

282.7 °F - closed cup

flash_point_c

139.3 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Structure Design of Multifunctional Furoate and Pyroglutamate Esters of Dextran by Polymer?Analogous Reactions.

Hornig S.

Macromolecular Bioscience, 7(3), 297-306 (2007)

A new orally active antidiabetic vanadyl complex-bis (α-furancarboxylato) oxovanadium (IV).

Xie M.

Journal of Inorganic Biochemistry, 99(2), 546-551 (2005)

A bell-shaped Mn11Gd2 single-molecule magnet.

Mereacre VM.

Journal of the American Chemical Society, 129(30), 9248-9249 (2007)

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Global Trade Item Number

SKU	GTIN
F20505-100G	04061833612712
F20505-500G	04061833612743
F20505-5G	04061833612750