2,2,6-Trifluoro-1,3-benzodioxol-5-amine is a chemical compound characterized by its unique structure, which includes a benzodioxole moiety substituted with trifluoromethyl and amino groups. This compound features three fluorine atoms attached to the carbon backbone, which significantly influences its chemical reactivity and physical properties, such as increased lipophilicity and potential bioactivity. The presence of the amino group suggests that it may participate in hydrogen bonding and can act as a nucleophile in various chemical reactions. The trifluoromethyl group often enhances the compound's stability and can affect its interaction with biological targets, making it of interest in medicinal chemistry and drug development. Additionally, the compound's specific arrangement of atoms contributes to its potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. As with many fluorinated compounds, it may exhibit unique solubility characteristics and environmental persistence, which are important considerations in its handling and application.

2,2,6-TRIFLUORO-1,3-BENZODIOXOL-5-AMINE

120934-03-4: 2,2,6-Trifluoro-1,3-benzodioxol-5-amine is a chemical compound characterized by its unique structure, which includes a benzodioxole moiety substituted with trifluoromethyl and amino groups. This compound features three fluorine atoms attached to the carbon backbone, which significantly influences its chemical reactivity and physical properties, such as increased lipophilicity and potential bioactivity. The presence of the amino group suggests that it may participate in hydrogen bonding and can act as a nucleophile in various chemical reactions. The trifluoromethyl group often enhances the compound's stability and can affect its interaction with biological targets, making it of interest in medicinal chemistry and drug development. Additionally, the compound's specific arrangement of atoms contributes to its potential applications in pharmaceuticals, agrochemicals, or as a building block in organic synthesis. As with many fluorinated compounds, it may exhibit unique solubility characteristics and environmental persistence, which are important considerations in its handling and application.

CAS 120934-03-4

2,2,6-TRIFLUORO-1,3-BENZODIOXOL-5-AMINE

2,2,6-Trifluorobenzo[d][1,3]dioxol-5-amine

Ref: IN-DA007PCV

2,2,6-Trifluoro-1,3-benzodioxol-5-amine

Ref: 54-PC103920

2,2,6-Trifluoro-benzo[1,3]dioxol-5-ylamine

Ref: 10-F032867