185922
Furan
≥99%
Synonym(s):
1,4-Epoxybuta-1,3-diene, Divinylene oxide, Oxacyclopentadiene, Oxole, Tetrole
About This Item
Recommended Products
vapor density
2.35 (vs air)
Quality Level
vapor pressure
1672 mmHg ( 55 °C)
31.66 psi ( 55 °C)
493 mmHg ( 20 °C)
9.22 psi ( 20 °C)
Assay
≥99%
form
liquid
contains
0.025 wt. % BHT as inhibitor
expl. lim.
14.3 %
refractive index
n20/D 1.421 (lit.)
bp
32 °C/758 mmHg (lit.)
solubility
alcohols: freely soluble
diethyl ether: freely soluble
water: insoluble
density
0.936 g/mL at 25 °C (lit.)
shipped in
wet ice
storage temp.
2-8°C
SMILES string
c1ccoc1
InChI
1S/C4H4O/c1-2-4-5-3-1/h1-4H
InChI key
YLQBMQCUIZJEEH-UHFFFAOYSA-N
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General description
Application
- Preparation of the starting material required for the synthesis of calix[6]pyrrole.
- To investigate the kinetics and mechanism of reactions of chlorine atoms with volatile organic compounds.
- Catalytic transformation of furan to aromatics and olefins.
Signal Word
Danger
Hazard Statements
Precautionary Statements
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
Supplementary Hazards
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
-32.8 °F - closed cup
Flash Point(C)
-36 °C - closed cup
Personal Protective Equipment
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Articles
The Diels–Alder reaction is the reaction between a conjugated diene and an alkene (dienophile) to form unsaturated six-membered rings. Since the reaction involves the formation of a cyclic product via a cyclic transition state, it is also referred to as a "cycloaddition".
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