Amino alcohols are compounds that contain both amino (-NH2) and hydroxyl (-OH) functional groups. The synthesis of fluorine-containing amino alcohols often starts with N-Substituted α-trifluoromethyl β-nitroamines as a key intermediate. The nitro group is reduced to an amino group, and subsequent chemical reactions can introduce the hydroxyl group at a suitable position, resulting in the desired amino alcohol. These compounds can be important building blocks in the synthesis of pharmaceuticals and agrochemicals.
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3,3,3-trifluoro-2-(N-phenylamino)propane-1-amine
2-(hydroxymethyl)-N-(2-methylbenzoyl)piperidine
Propanoic acid, 3-[[(1,1-dimethylethoxy)carbonyl]amino]-2-hydroxy-, methyl
N-cyclohexyl-1,1-dimethyl-L-valinol
2-amino-2-methylbutanesulfonic acid
(S,E)-(-)-3-cyclohexyl-1-phenylprop-2-en-1-ol
Urea, N,N'-bis(3-hydroxypropyl)-
N-(1-hydroxy-2-methylpropan-2-yl)-4-methylbenzenesulfinamide
2-[benzyl(prop-2-yn-1-yl)amino]ethanol
