186988
2-Ethylfuran
97%
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About This Item
Empirical Formula (Hill Notation):
C6H8O
CAS Number:
Molecular Weight:
96.13
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
221-714-0
MDL number:
Assay:
97%
Form:
liquid
Product Name
2-Ethylfuran, 97%
InChI key
HLPIHRDZBHXTFJ-UHFFFAOYSA-N
InChI
1S/C6H8O/c1-2-6-4-3-5-7-6/h3-5H,2H2,1H3
SMILES string
CCc1ccco1
assay
97%
form
liquid
refractive index
n20/D 1.439 (lit.)
bp
92-93 °C/768 mmHg (lit.)
density
0.912 g/mL at 25 °C (lit.)
Quality Level
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Application
2-Ethylfuran was used to investigate the gas phase products formed from the Cl atoms initiated reactions of 2-ethylfuran by in situ long-path FTIR absorption spectroscopy. It was also used in the synthesis of 4-oxo-(E)-2-hexenal via ring opening reaction using aqueous N-bromosuccinimide.
General description
2-Ethylfuran undergoes tetraphenylporphin-photosensitized oxygenation in non-polar aprotic solvents via (4+2)-cycloaddition of singlet oxygen to yield the corresponding monomeric unsaturated secondary ozonide.
signalword
Danger
hcodes
Hazard Classifications
Flam. Liq. 2
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
28.4 °F - closed cup
flash_point_c
-2 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Atmospheric degradation of alkylfurans with chlorine atoms: Product and mechanistic study.
Villanueva F, et al.
Atmospheric Environment, 43(17), 2804-2813 (2009)
Singlet oxygen photooxygenation of furans: Isolation and reactions of (4+ 2)-cycloaddition products (unsaturated sec.-ozonides).
Gollnick K and Griesbeck A.
Tetrahedron, 41(11), 2057-2068 (1985)
Koji Noge et al.
Journal of chemical ecology, 38(8), 1050-1056 (2012-10-12)
We examined whether shared volatiles found in various heteropteran species and developmental stages function to repel predators. The nymphal dorsal abdominal gland secretions of Riptortus pedestris (Heteroptera: Alydidae) and Thasus acutangulus (Heteroptera: Coreidae), and the metathoracic scent gland secretion of
Francisco J Hidalgo et al.
Journal of agricultural and food chemistry, 62(49), 12045-12051 (2014-11-25)
The carbonyl-scavenging ability of 2-amino-1-methylbenzimidazole (AMBI) and the heterocyclic aromatic amine 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine (PhIP) was investigated in an attempt to identify new routes that can modify the carbonyl content of foods. The reaction of both AMBI and PhIP with 2-alkenals, 2,4-alkadienals
Audrey R Smith et al.
Journal of mass spectrometry : JMS, 50(11), 1206-1213 (2015-10-28)
Absolute photoionization cross sections of the molecules 2-ethylfuran, 2-acetylfuran and furfural, including partial ionization cross sections for the dissociative ionized fragments, are measured for the first time. These measurements are important because they allow fuel quantification via photoionization mass spectrometry
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