Furfurylamine
Furfurylamine is an aromatic amine typically formed by the reductive amination of furfural with ammonia.
Names | |
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IUPAC name
1-(2-Furyl)methylamine | |
Other names
furfurylamine, 2-Aminomethylfuran | |
Identifiers | |
3D model (JSmol) |
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ChemSpider | |
ECHA InfoCard | 100.009.580 |
EC Number |
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PubChem CID |
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UNII | |
UN number | 2526 |
CompTox Dashboard (EPA) |
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Properties | |
C5H7NO | |
Molar mass | 97.117 g·mol−1 |
Density | 1.099 g/mL liquid |
Melting point | −70 °C (−94 °F; 203 K) |
Boiling point | 145 °C (293 °F; 418 K) |
Soluble | |
Hazards | |
GHS pictograms | |
GHS Signal word | Danger |
H226, H301, H302, H310, H311, H312, H314, H332 | |
P210, P233, P240, P241, P242, P243, P260, P261, P262, P264, P270, P271, P280, P301+310, P301+312, P301+330+331, P302+350, P302+352, P303+361+353, P304+312, P304+340, P305+351+338, P310, P312, P321 | |
Flash point | 37 °C (99 °F; 310 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
The pharmaceutical drug furtrethonium, a parasympathomimetic cholinergic, is a trimethyl ammonium derivative of furfurylamine.
Furfurylamine also has use in the synthesis of Barmastine.
See also
- 2-Furonitrile - corresponding nitrile
- Furan-2-ylmethanethiol - corresponding thiol
- Furfuryl alcohol - corresponding alcohol
- 2-Furoic acid - corresponding carboxylic acid
References
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