AH94997
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $10.00 | $7.00 | - + | |
250mg | 95% | in stock | $17.00 | $12.00 | - + | |
1g | 95% | in stock | $51.00 | $36.00 | - + | |
5g | 95% | in stock | $127.00 | $89.00 | - + | |
25g | 96% | in stock | $550.00 | $385.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AH94997 |
Chemical Name: | 6-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one |
CAS Number: | 881189-74-8 |
Molecular Formula: | C9H6BrFO |
Molecular Weight: | 229.0457 |
MDL Number: | MFCD14654077 |
SMILES: | Brc1cc(F)c2c(c1)C(=O)CC2 |
6-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one is a versatile compound widely utilized in chemical synthesis due to its unique reactivity and structural properties. This compound serves as a valuable building block in organic synthesis, offering a range of applications in the preparation of various functionalized indenone derivatives. Its chemical structure, characterized by the presence of both bromine and fluorine substituents on the indenone scaffold, enables the selective introduction of these functional groups into target molecules during synthetic transformations.In chemical synthesis, 6-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one can be employed as a key intermediate for the construction of more complex organic compounds. Its strategic placement of bromine and fluorine atoms allows chemists to perform selective substitutions, additions, and functional group manipulations, facilitating the synthesis of diverse organic molecules. Furthermore, the indenone framework provides a rigid and stable structure that can enhance the overall reactivity and stability of the intermediates and final products in synthetic pathways.Moreover, the presence of bromine and fluorine substituents in 6-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one imparts unique physicochemical properties, such as altered electronic characteristics and increased nucleophilicity. These features can be harnessed to enable specific reactions, such as nucleophilic substitutions, aromatic functionalization, and cross-coupling reactions, in the design and synthesis of novel organic compounds. Overall, the utility of 6-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one in chemical synthesis highlights its significance as a valuable tool for accessing diverse chemical space and developing innovative synthetic methodologies.