AE48426
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 98% | in stock | $76.00 | $54.00 | - + | |
250mg | 98% | in stock | $129.00 | $91.00 | - + | |
1g | 98% | in stock | $425.00 | $298.00 | - + | |
5g | 98% | in stock | $1,996.00 | $1,397.00 | - + | |
10g | 98% | in stock | $3,302.00 | $2,311.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AE48426 |
Chemical Name: | 6-Bromo-4-fluoroindolin-2-one |
CAS Number: | 1000341-00-3 |
Molecular Formula: | C8H5BrFNO |
Molecular Weight: | 230.0338032 |
MDL Number: | MFCD09880178 |
SMILES: | O=C1Nc2c(C1)c(F)cc(c2)Br |
Complexity: | 211 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 1.6 |
6-Bromo-4-fluoroindolin-2-one is a versatile compound that finds widespread application in chemical synthesis processes. Due to its unique structure and reactivity, this compound is commonly used as a key building block in the preparation of complex organic molecules. Its strategic placement of bromine and fluorine atoms makes it particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.In organic synthesis, 6-Bromo-4-fluoroindolin-2-one serves as a valuable intermediate for the construction of heterocyclic compounds. Its ability to undergo various functional group transformations, such as nucleophilic substitution and palladium-catalyzed cross-coupling reactions, makes it an essential tool for chemists seeking to create novel molecular structures. Additionally, the presence of both bromine and fluorine substituents provides synthetic chemists with opportunities for further diversification through selective functionalization strategies.Furthermore, 6-Bromo-4-fluoroindolin-2-one can participate in cascade reactions and multi-step synthetic sequences, enabling the efficient formation of complex molecular architectures. Its compatibility with a wide range of reaction conditions and its tolerance to diverse functional groups make it a valuable resource in the toolbox of synthetic chemists looking to streamline their synthetic routes and access intricate molecular frameworks.Overall, the utility of 6-Bromo-4-fluoroindolin-2-one in chemical synthesis lies in its versatility, reactivity, and compatibility with various synthetic methodologies. By harnessing the unique properties of this compound, chemists can access a diverse array of molecular structures with potential applications in pharmaceuticals, materials science, and other areas of chemical research.