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Merck
CN

F19558

Furan

98%

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About This Item

Empirical Formula (Hill Notation):
C4H4O
CAS Number:
110-00-9
Molecular Weight:
68.07
EC Number:
203-727-3
UNSPSC Code:
12352100
PubChem Substance ID:
329799690
Beilstein/REAXYS Number:
103221
MDL number:
MFCD00003222
Assay:
98%

Key Documents

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vapor density

2.35 (vs air)

vapor pressure

1672 mmHg ( 55 °C), 31.66 psi ( 55 °C), 493 mmHg ( 20 °C), 9.22 psi ( 20 °C)

assay

98%

contains

0.025 wt. % BHT as inhibitor

expl. lim.

14.3 %

refractive index

n20/D 1.421 (lit.)

bp

32 °C/758 mmHg (lit.)

density

0.936 g/mL at 25 °C (lit.)

SMILES string

c1ccoc1

InChI

1S/C4H4O/c1-2-4-5-3-1/h1-4H

InChI key

YLQBMQCUIZJEEH-UHFFFAOYSA-N

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Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Carc. 1B - Flam. Liq. 1 - Muta. 2 - Skin Irrit. 2 - STOT RE 2

supp_hazards

EUH019

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_f

-32.8 °F - closed cup

flash_point_c

-36 °C - closed cup

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
06520PH
S43800
S08580
10228HE
03822DT

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Prashant Sonar et al.
Chemical communications (Cambridge, England), 49(16), 1588-1590 (2012-11-09)
A fluorenone based alternating copolymer () with a furan based fused aromatic moiety has been designed and synthesized. exhibits a small band gap with a lower HOMO value. Testing this polymer semiconductor as the active layer in organic thin-film transistors
Rialet Pieters et al.
Environment international, 66, 71-78 (2014-02-18)
In South Africa, 26-50% of households use solid fuel for cooking food and heating houses. When used as fuel, wood and chlorinated waste are known sources of polychlorinated dibenzo-para-dioxins, polychlorinated dibenzofurans (PCDD/Fs), and polychlorinated biphenyls (PCBs). Here, we compare PCDD/F
C W Heppner et al.
Food additives and contaminants, 24 Suppl 1, 114-121 (2007-09-22)
Furan is an organic, volatile compound used in various chemical-manufacturing industries. Headspace gas chromatography is the analytical method of choice for obtaining reliable results on its occurrence. The presence of furan in some food items has been known since the
Carolin Neuwirth et al.
Molecular nutrition & food research, 56(9), 1363-1374 (2012-08-07)
Furan is a potent hepatotoxicant and liver carcinogen in rodents. However, short-term tests for genotoxicity of furan are inconclusive. The aim of this study was to assess the potential of furan to covalently bind to DNA, and to assess furan
Joseph Salamoun et al.
Organic letters, 16(7), 2034-2037 (2014-03-20)
Two complementary approaches for the preparation of linked 5-membered heterocycles were developed. The Pd-catalyzed Suzuki-Miyaura cross-coupling with halogenated furan, thiophene, and selenophene led to higher overall yields, but C,H-bond activation was a more efficient strategy for the coupling at C(2)
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