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About This Item
Empirical Formula (Hill Notation):
C5H6O
CAS Number:
Molecular Weight:
82.10
Beilstein/REAXYS Number:
103733
EC Number:
Council of Europe no.:
2209
MDL number:
UNSPSC Code:
12164502
Flavis number:
13.030
Recommended Products
biological source
synthetic
grade
Kosher
vapor density
2.8 (vs air)
vapor pressure
139 mmHg ( 20 °C)
561 mmHg ( 55 °C)
assay
≥98%
contains
≤300 ppm BHT as stabilizer
refractive index
n20/D 1.433 (lit.)
bp
63-66 °C (lit.)
density
0.91 g/mL at 25 °C (lit.)
organoleptic
ethereal
SMILES string
Cc1ccco1
InChI
1S/C5H6O/c1-5-3-2-4-6-5/h2-4H,1H3
InChI key
VQKFNUFAXTZWDK-UHFFFAOYSA-N
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Jiao Huo et al.
Mutation research, 854-855, 503209-503209 (2020-07-15)
We have measured the toxicity and genotoxicity of 2-methylfuran, which is formed in foods during thermal processing. The agent was administered by oral gavage to male Sprague-Dawley rats, daily for 28 days, before performing general toxicology analysis and the following
Luca Cappelletti et al.
Ultrasonics sonochemistry, 27, 30-36 (2015-07-19)
An ultrasound-assisted three-component, one-pot domino reaction with ferrocenecarboxaldehyde is herein reported. The sequence of reactions entails the allylindation and dehydrative alkylation of stabilized C-nucleophiles (e.g. electron-rich-(hetero)aromatics and stabilized enols) and N-nucleophiles (e.g. azoles). Sonochemical reactions have been performed in three
Hanna Valolahti et al.
Global change biology, 21(9), 3478-3488 (2015-05-23)
Emissions of biogenic volatile organic compounds (BVOCs) have been earlier shown to be highly temperature sensitive in subarctic ecosystems. As these ecosystems experience rapidly advancing pronounced climate warming, we aimed to investigate how warming affects the BVOC emissions in the
Maryam Chaichi et al.
Food additives & contaminants. Part B, Surveillance, 8(1), 73-80 (2014-10-31)
In this study, the levels of furan, 2-methylfuran, 2,5-dimethylfuran, vinyl furan, 2-methoxymethyl-furan and furfural in different coffee products were evaluated. Simultaneous determination of these six furanic compounds was performed by a head space liquid-phase micro-extraction (HS-LPME) method. A total of
Benjamin Sachse et al.
Carcinogenesis, 35(10), 2339-2345 (2014-07-24)
Furfuryl alcohol is a rodent carcinogen present in numerous foodstuffs. Sulfotransferases (SULTs) convert furfuryl alcohol into the DNA reactive and mutagenic 2-sulfoxymethylfuran. Sensitive techniques for the isotope-dilution ultra performance liquid chromatography-tandem mass spectrometry quantification of resulting DNA adducts, e.g. N
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