(R)-(-)-Tetrahydrofurfurylamine

CAS: 7202-43-9

Ref. 3D-FT60310

Product Information

• Name: (R)-(-)-Tetrahydrofurfurylamine
• Synonyms: (R)-(-)-2-(Aminomethyl)tetrahydrofuran, (2R)-2-Aminomethyltetrahydrofuran, (2R)-Tetrahydro-2-furanmethanamine, (2R)-Tetrahydrofuran-2-methanamine, (R)-(tetrahydrofuran-2-yl)methanamine, (R)-1-(Tetrahydrofuran-2-yl)methanamine, (R)-1-(Tetrahydrofuran-2-yl)methylamine, (R)-2-Tetrahydrofurfurylamine, (R)-Tetrahydrofuran-2-ylmethylamine, 1-[(2R)-Oxolan-2-yl]methanamine, 1-[(2R)-tetrahydrofuran-2-yl]methanamine, 2-Furanmethanamine tetrahydro-, (2R)-, 2-Furanmethanamine, tetrahydro-, (R)-, Furfurylamine, tetrahydro-, (R)-, [((R)-Tetrahydrofuran-2-yl)methyl]amine, [(2R)-Oxolan-2-yl]methanamine, [(R)-1-(Tetrahydro-furan-2-yl)]-methylamine, [[(2R)-Tetrahydro-2-furanyl]methyl]amine
• CAS: 7202-43-9

Description

Tetrahydrofuranamine is an enamine that can exist in two tautomeric forms, the keto form and the enol form. It is a chiral molecule with four stereogenic centres. The keto form is more stable than the enol form due to resonance stabilization. Tetrahydrofuranamine has been synthesized by reacting l-tartaric acid with ammonia and hydrogen chloride. This reaction produces an imine, which upon heating to 160°C converts to (R)-(-)-tetrahydrofurfurylamine in high yield. This compound can be used as a precursor for other compounds such as cyclopentanol or dihydropyranone.

• Brand: Biosynth

Chemical properties

• Molecular weight: 101.15 g/mol
• Formula: C₅H₁₁NO
• Purity: Min. 95%
• InChI: InChI=1S/C5H11NO/c6-4-5-2-1-3-7-5/h5H,1-4,6H2/t5-/m1/s1
• InChI key: InChIKey=YNOGYQAEJGADFJ-RXMQYKEDSA-N
• SMILES: NC[C@H]1CCCO1