The chemical substance known as (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one, with the CAS number 781650-41-7, is a member of the azepane class of compounds, characterized by a seven-membered saturated ring containing nitrogen. This compound features a chiral center, indicated by its (3R,6S) configuration, which contributes to its stereochemical properties and potential biological activity. The presence of an amino group and a carbonyl group in its structure suggests that it may exhibit properties typical of amides, including potential interactions with biological targets. The incorporation of difluorophenyl and trifluoroethyl groups enhances its lipophilicity and may influence its pharmacokinetic properties, making it of interest in medicinal chemistry. Such fluorinated compounds often exhibit increased metabolic stability and altered binding affinities, which can be advantageous in drug design. Overall, this compound's unique structural features may contribute to its potential applications in pharmaceuticals or agrochemicals, although specific biological activities would require further investigation.

(3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one

781650-41-7: The chemical substance known as (3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one, with the CAS number 781650-41-7, is a member of the azepane class of compounds, characterized by a seven-membered saturated ring containing nitrogen. This compound features a chiral center, indicated by its (3R,6S) configuration, which contributes to its stereochemical properties and potential biological activity. The presence of an amino group and a carbonyl group in its structure suggests that it may exhibit properties typical of amides, including potential interactions with biological targets. The incorporation of difluorophenyl and trifluoroethyl groups enhances its lipophilicity and may influence its pharmacokinetic properties, making it of interest in medicinal chemistry. Such fluorinated compounds often exhibit increased metabolic stability and altered binding affinities, which can be advantageous in drug design. Overall, this compound's unique structural features may contribute to its potential applications in pharmaceuticals or agrochemicals, although specific biological activities would require further investigation.

(3R,6S)-3-Amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one

<p>(3R,6S)-3-Amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one</p>

CAS 781650-41-7

(3R,6S)-3-amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one

(3R,6S)-3-Amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one

Ref: IN-DA00GIFB

(3R,6S)-3-Amino-6-(2,3-difluorophenyl)-1-(2,2,2-trifluoroethyl)azepan-2-one

Ref: 54-PC448048