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Key Documents

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W501506

Sigma-Aldrich

2-Furoic acid

≥97%

Sinónimos:

Furan-2-carboxylic acid

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About This Item

Fórmula empírica (notación de Hill):
C5H4O3
Número de CAS:
88-14-2
Peso molecular:
112.08
Beilstein/REAXYS Number:
110149
EC Number:
201-803-0
MDL number:
MFCD00003238
UNSPSC Code:
12164502
Flavis number:
13.136

assay

≥97%

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

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Features and Benefits

Odorless

Other Notes

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

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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Certificados de análisis (COA)

Lot/Batch Number
11429PU
05221AS
01131CV
32013
F912

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Chun-Yuan Li et al.
Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials, 31(5), 645-647 (2008-10-02)
The metabolites of a marine streptomyces sp. actinomycete (No. 195-02) were studied and eight compounds were isolated from the fermentation liquid, structures were elucidated by spectroscopy methods as p-hydroxy-benzonitrile (1), 2-methyl-furan-3-carboxylic acid(2), furan-2-carboxylic acid (3), cyclo(Phe-Phe) (4), cyclo(Leu-Ileu) (5), nicotinic
María C Rodríguez-Argüelles et al.
Journal of inorganic biochemistry, 103(1), 35-42 (2008-10-25)
Cobalt, nickel, copper and zinc coordination compounds of two thiosemicarbazones with general composition ML(2) (L: monodeprotonated ligand corresponding to 2-acetyl-gamma-butyrolactone thiosemicarbazone, HL(1), and 2-furancarbaldehyde thiosemicarbazone, HL(2)) and also complexes with general composition MCl(2)(HL(2)) were synthesized (except [NiCl(2)(HL(2))] and [Co(L(2))(2)]). The
Z B Tan et al.
Journal of analytical toxicology, 27(1), 43-46 (2003-02-18)
An improved high-performance liquid chromatographic (HPLC) method for the analysis of the metabolite furoic acid in the urine of workers occupationally exposed to furfural is described. The procedure involved an alkaline hydrolysis step followed by solvent extraction using ethyl acetate.
Hiroshi Yanagita et al.
Bioorganic & medicinal chemistry, 19(2), 816-825 (2011-01-05)
Rapid emergence of drug-resistant variants is one of the most serious problems in chemotherapy for HIV-1 infectious diseases. Inhibitors acting on a target not addressed by approved drugs are of great importance to suppress drug-resistant viruses. HIV-1 reverse transcriptase has
H B Klinke et al.
Applied microbiology and biotechnology, 57(5-6), 631-638 (2002-01-10)
Alkaline wet oxidation (WO) (using water, 6.5 g/l sodium carbonate, and 12 bar oxygen at 195 degrees C) was used for pre-treating wheat straw (60 g/l), resulting in a hemicellulose-rich hydrolysate and a cellulose-rich solid fraction. The hydrolysate consisted of
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