F20505
2-Furoic acid
98%
Synonym(s):
Furan-2-carboxylic acid
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About This Item
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Quality Level
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
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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.
signalword
Danger
hcodes
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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Syntheses, crystal structure and luminescence property of novel 4f-3d heterometallic one-dimensional coordination polymers.
Journal of Physics and Chemistry of Solids, 67(7), 1372-1378 (2006)
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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 new orally active antidiabetic vanadyl complex-bis (α-furancarboxylato) oxovanadium (IV).
Journal of Inorganic Biochemistry, 99(2), 546-551 (2005)
A bell-shaped Mn11Gd2 single-molecule magnet.
Journal of the American Chemical Society, 129(30), 9248-9249 (2007)
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