1H-Isoindol-1-one, 6-amino-2-(1,3-benzodioxol-5-ylmethyl)-4-bromo-2,3-dihydro- is a chemical compound characterized by its isoindole structure, which features a fused bicyclic system. The presence of an amino group at the 6-position and a bromo substituent at the 4-position contributes to its reactivity and potential biological activity. The compound also contains a 1,3-benzodioxole moiety, which is known for its role in various pharmacological activities. This compound is typically studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its unique structural features that may interact with biological targets. Its molecular structure suggests it may exhibit properties such as fluorescence or specific binding affinities, making it of interest in both synthetic and medicinal chemistry research. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups.

1H-Isoindol-1-one, 6-aMino-2-(1,3-benzodioxol-5-ylMethyl)-4-broMo-2,3-dihydro-

169043-96-3: 1H-Isoindol-1-one, 6-amino-2-(1,3-benzodioxol-5-ylmethyl)-4-bromo-2,3-dihydro- is a chemical compound characterized by its isoindole structure, which features a fused bicyclic system. The presence of an amino group at the 6-position and a bromo substituent at the 4-position contributes to its reactivity and potential biological activity. The compound also contains a 1,3-benzodioxole moiety, which is known for its role in various pharmacological activities. This compound is typically studied for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its unique structural features that may interact with biological targets. Its molecular structure suggests it may exhibit properties such as fluorescence or specific binding affinities, making it of interest in both synthetic and medicinal chemistry research. As with many organic compounds, its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other functional groups.

6-Amino-2-(benzo[d][1,3]dioxol-5-ylmethyl)-4-bromoisoindolin-1-one

<p>6-Amino-2-(1,3-benzodioxol-5-ylmethyl)-4-bromo-2,3-dihydro-1H-isoindol-1-one</p>

CAS 169043-96-3

1H-Isoindol-1-one, 6-aMino-2-(1,3-benzodioxol-5-ylMethyl)-4-broMo-2,3-dihydro-

6-Amino-2-(benzo[d][1,3]dioxol-5-ylmethyl)-4-bromoisoindolin-1-one

Ref: IN-DA001YG9

6-Amino-2-(1,3-benzodioxol-5-ylmethyl)-4-bromo-2,3-dihydro-1H-isoindol-1-one

Ref: 54-OR305275

6-Amino-2-(benzo[d][1,3]dioxol-5-ylmethyl)-4-bromoisoindolin-1-one

Ref: 10-F752537