These are organic compounds containing two amino groups (-NH2) separated by a single carbon atom. N-Substituted α-trifluoromethyl β-nitroamines can serve as valuable precursors for synthesizing fluorine-containing 1,2-diamines. The process typically involves the reduction of the nitro group (-NO2) in the starting compound to the corresponding amino group (-NH2). The α-trifluoromethyl substituent can provide desirable chemical properties, such as increased stability and bioavailability in medicinal compounds.
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3,3,3-trifluoro-2-(N-phenylamino)propane-1-amine
3-(3-methoxybenzyl)-1,4-dimethyl-3-(trifluoromethyl)piperazin-2-one
((S)-2-Benzyloxycarbonylamino-4-isocyanato-butyl)-carbamic acid benzyl ester
C18H17N3O
