L-Valinol

CAS: 2026-48-4

Ref. 3D-FV10652

Información del producto

• Nombre: L-Valinol
• Sinónimos: (S)-(+)-2-Amino-3-methyl-1-butanol, (+)-(S)-Valinol, (+)-2-Amino-3-methyl-1-butanol, (+)-Valinol, (2S)-1-Hydroxy-3-methylbutan-2-amine, (2S)-2-Amino-3-methyl-1-butanol, (2S)-Valinol, (S)-2-Amino-3-methylbutanol, 1-Butanol, 2-amino-3-methyl-, (S)-, 1-Butanol, 2-amino-3-methyl-, <span class="text-smallcaps">L</span>-, 1-Butanol, 2-amino-3-methyl-, L-, <span class="text-smallcaps">L</span>-Valinol, Butanol, 2-Amino-3-Methyl, (S)-(+)-, L-2-amino-3-methylbutan-1-ol, L-2-amino-3-methylbutane-1-ol, L-2-amino-3-metilbutan-1-ol, Nsc 322922, [(S)-1-(Hydroxymethyl)-2-methylpropyl]amine
• CAS: 2026-48-4

Descripción

L-Valinol is a model system that is used to study the reaction of aziridines with oxygen nucleophiles. It has been shown that this reaction proceeds through the formation of an intermediate, hydrogen tartrate, followed by a second step with nitrogen atoms as the nucleophile and alcohol residue as the substrate. The use of L-valinol in asymmetric synthesis was also demonstrated. In this process, amides were obtained with high enantioselectivity by reacting L-valinol with amines in acidic conditions. This synthetic pathway was found to be synergic with other reactions, such as nitroolefination and benzoylation.

• Marca: Biosynth

Propiedades químicas

• Peso molecular: 103.16 g/mol
• Fórmula: C₅H₁₃NO
• Pureza: Min. 95%
• Color/Forma: Solidified Mass
• InChI: InChI=1S/C5H13NO/c1-4(2)5(6)3-7/h4-5,7H,3,6H2,1-2H3/t5-/m1/s1
• Clave InChI: InChIKey=NWYYWIJOWOLJNR-RXMQYKEDSA-N
• SMILES: CC(C)[C@H](N)CO