W501506
2-Furoic acid
≥97%
Synonym(s):
Furan-2-carboxylic acid
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About This Item
Empirical Formula (Hill Notation):
C5H4O3
CAS Number:
Molecular Weight:
112.08
Beilstein:
110149
EC Number:
MDL number:
UNSPSC Code:
12164502
Flavis number:
13.136
Recommended Products
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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Signal Word
Danger
Hazard Statements
Precautionary Statements
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
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[Secondary metabolites of a marine actinomycete Streptomyces sp. (No. 195-02) from South China Sea].
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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