| Weight | 97.117 g/mol |
|---|---|
| Formula | C5H7NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 1 |
Furfurylamine (617-89-0)
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- Synthesis and copolymerization of fully bio-based benzoxazines from guaiacol, furfurylamine and stearylamine (Green Chemistry, 2012)
- Nickel(II) and copper(II) complexes with an asymmetric bidentate Schiff-base ligand derived from furfurylamine (Journal of Thermal Analysis and Calorimetry, 2011)
- Synthesis, structure and antibacterial activity of manganese(III) complexes of a Schiff base derived from furfurylamine (Polyhedron, 2009)
- Reductive amination of furfural to furfurylamine using aqueous ammonia solution and molecular hydrogen: an environmentally friendly approach (Green Chemistry, 2016)
- Synthesis of Difurfuryl Diamines by the Acidic Condensation of Furfurylamine with Aldehydes and Their Mechanism of Formation (Journal of Organic Chemistry, 1995)
- 1,2-Dihydroisoindolines from Intramolecular [4+2] Cycloaddition of N-Allyl-2-Furfurylamine Halohydrates (Synthetic Communications, 1988)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=COC(=C1)CN
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InChIKeyDDRPCXLAQZKBJP-UHFFFAOYSA-N
- Pubchem - Furfurylamine
- Wikipedia - furfurylamine
Furfurylamine is an aromatic amine typically formed by the reductive amination of furfural with ammonia. The pharmaceutical drug furtrethonium, a parasympathomimetic cholinergic, is a derivative of furfurylamine. Furfurylamine also has use in the synthesis of Barmastine.
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Furfurylamine
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