4-(Trifluoroacetylamino)-1-butanol is an organic compound characterized by the presence of a butanol backbone with a trifluoroacetylamino group. This compound features a hydroxyl (-OH) group, which contributes to its potential as a solvent and its ability to participate in hydrogen bonding. The trifluoroacetylamino moiety introduces significant electronegativity due to the presence of three fluorine atoms, which can influence the compound's reactivity and polarity. This structure may enhance its solubility in polar solvents and affect its interactions with biological systems, making it of interest in medicinal chemistry. The compound is likely to exhibit moderate stability under standard conditions, but its reactivity can vary depending on the presence of other functional groups or environmental factors. Additionally, the trifluoroacetyl group may impart unique properties, such as increased lipophilicity or altered metabolic pathways, which could be relevant in drug design and development. Overall, 4-(trifluoroacetylamino)-1-butanol presents a unique combination of functional groups that can be leveraged in various chemical applications.

4-(trifluoroacetylamino)-1-butanol

128238-43-7: 4-(Trifluoroacetylamino)-1-butanol is an organic compound characterized by the presence of a butanol backbone with a trifluoroacetylamino group. This compound features a hydroxyl (-OH) group, which contributes to its potential as a solvent and its ability to participate in hydrogen bonding. The trifluoroacetylamino moiety introduces significant electronegativity due to the presence of three fluorine atoms, which can influence the compound's reactivity and polarity. This structure may enhance its solubility in polar solvents and affect its interactions with biological systems, making it of interest in medicinal chemistry. The compound is likely to exhibit moderate stability under standard conditions, but its reactivity can vary depending on the presence of other functional groups or environmental factors. Additionally, the trifluoroacetyl group may impart unique properties, such as increased lipophilicity or altered metabolic pathways, which could be relevant in drug design and development. Overall, 4-(trifluoroacetylamino)-1-butanol presents a unique combination of functional groups that can be leveraged in various chemical applications.

CAS 128238-43-7

4-(trifluoroacetylamino)-1-butanol

4-(Trifluoroacetylamino)-1-butanol

Ref: IN-DA000XVN

2,2,2-Trifluoro-N-(4-hydroxybutyl)acetamide

Ref: 54-PC251337