| Weight | 101.149 g/mol |
|---|---|
| Formula | C5H11NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Tetrahydrofurfurylamine (4795-29-3)
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- Spectroscopic studies and PM5 semiempirical calculations of tautomeric forms of gossypol schiff base with (R)-tetrahydrofurfurylamine (Journal of Molecular Structure, 2004)
- Excess enthalpies of mixtures containing tetrahydrofurfurylalcohol or tetrahydrofurfurylamine (The Journal of Chemical Thermodynamics, 1978)
- ESI MS and PM5 semiempirical studies of gossypol schiff base with (R)-tetrahydrofurfurylamine complexes and monovalent cations (Journal of Molecular Structure, 2004)
- Synthesis and solid state structures of two new copper(II) complexes of Schiff bases derived from furfuryl and tetrahydrofurfurylamine (Russian Journal of Coordination Chemistry, 2010)
- Synthesis, structure and urease inhibition studies of dimeric copper(II) complexes with a tridentate Schiff base ligand derived from tetrahydrofurfurylamine (Inorganica Chimica Acta, 2013)
- 5, 5'-(oxydimethylene) bis-tetrahydrofurfurylamine (1961)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC(OC1)CN
-
InChIKeyYNOGYQAEJGADFJ-UHFFFAOYSA-N
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Estimated Properties
| Boiling Point | 141.56 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 148.8 C | EPI Suite |
| Density | 0.99 g/cm3 | EPA T.E.S.T. |
| Flash Point | 37.07 C | EPA T.E.S.T. |
| Melting Point | -16.55 C | EPI Suite |
| Water Solubility | 161331 mg/L | EPA T.E.S.T. |
| Water Solubility | 1e+06 mg/L | EPI Suite |
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