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Merck
CN

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
EC Number:
201-803-0
UNSPSC Code:
12164502
Flavis number:
13.136
Beilstein/REAXYS Number:
110149
MDL number:
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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

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1C

Storage Class

8A - Combustible corrosive hazardous materials

wgk

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

Regulatory Information

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K Suthindhiran et al.
Natural product research, 25(8), 834-843 (2011-04-05)
The antiviral activity of furan-2-yl acetate (C₆H₆O₃) extracted from Streptomyces VITSDK1 spp. was studied in cultured Sahul Indian Grouper Eye (SIGE) cells infected with fish nodavirus (FNV). The nodavirus infection in the SIGE cells was confirmed by reverse transcriptase-polymerase chain
Nadia Spano et al.
Talanta, 78(1), 310-314 (2009-01-29)
In this study 5-hydroxymethyl-2-furaldehyde (HMF), 2-furaldehyde, 3-furaldehyde, 2-furoic acid and 3-furoic acid are contemporarily determined in honey using a swift and direct RP-HPLC approach. The validation protocol was performed in terms of detection and quantification limits, precision (by repeatability and
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
Nancy N Nichols et al.
FEMS microbiology letters, 284(1), 52-57 (2008-05-22)
Pseudomonas putida Fu1 metabolizes furfural through a pathway involving conversion to 2-oxoglutarate, via 2-furoic acid (FA) and coenzyme A intermediates. Two P. putida transposon mutants were isolated that had impaired growth on furfural and FA, and DNA flanking the transposon
H B Klinke et al.
Biotechnology and bioengineering, 81(6), 738-747 (2003-01-17)
Alkaline wet oxidation (WO) (using water, 6.5 g/L sodium carbonate and 12 bar oxygen at 195 degrees C) was used as pretreatment method for wheat straw (60 g/L), resulting in a hydrolysate and a cellulosic solid fraction. The hydrolysate consisted

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