![1-butylbenzo[cd]indol-2(1H)-one](https://www.chemshuttle.com/media/catalog/product/cache/31dbf0bffbfa69a5826a72cec9a446de/1/8/189357_1.jpg)
6-bromobenzo[cd]indol-2(1H)-one
$300.00
CAS No.: 24856-00-6
Catalog No.: 197709
Purity: 95%
MF: C11H6BrNO
MW: 248.079
Storage: 2-8 degree Celsius
SMILES: BrC=1C=2C3=C(C(NC3=CC1)=O)C=CC2
Catalog No.: 197709
Purity: 95%
MF: C11H6BrNO
MW: 248.079
Storage: 2-8 degree Celsius
SMILES: BrC=1C=2C3=C(C(NC3=CC1)=O)C=CC2
6-bromobenzo[cd]indol-2(1H)-one; CAS No.: 24856-00-6;6-bromobenzo[cd]indol-2(1H)-one. PROPERTIES: 6-bromobenzo[cd]indol-2(1H)-one is a brominated indole derivative with a molecular weight of 287.07 g/mol. This pale yellow crystalline solid has a melting point between 210-213 C. The molecule features a benzo[cd]indole ring system with a bromo substituent at position 6 and a ketone group at position 2. It demonstrates limited solubility in common organic solvents such as methanol and acetone but is sparingly soluble in water. Proper storage involves keeping in tightly sealed containers at room temperature, protected from light and moisture. Safety considerations include the bromine substituent's potential to cause skin irritation and the ketone group's moderate toxicity. Proper protective equipment should be utilized during handling. APPLICATIONS: This compound primarily functions as a building block in the synthesis of agrochemicals and pharmaceuticals, where the brominated indole structure provides versatile sites for cross-coupling reactions. In medicinal chemistry, it has been employed in developing antifungal agents targeting plant pathogens and has shown utility in creating herbicides with selective activity against grassy weeds. The indole-2-one scaffold has also been explored in materials science for developing organic semiconductors, leveraging the extended conjugation to enhance charge carrier mobility. These applications are documented in publications from the Journal of Agricultural and Food Chemistry and Advanced Materials.
Reviews
Write Your Own Review