AA14549
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
100mg | 95% | in stock | $72.00 | $50.00 | - + | |
250mg | 95% | in stock | $155.00 | $108.00 | - + | |
1g | 95% | in stock | $422.00 | $295.00 | - + | |
5g | 95% | in stock | $1,422.00 | $995.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA14549 |
Chemical Name: | 6-Bromo-7-fluoro-3,4-dihydro-2H-1,4-benzoxazine |
CAS Number: | 1160102-28-2 |
Molecular Formula: | C8H7BrFNO |
Molecular Weight: | 232.0496832 |
MDL Number: | MFCD20441785 |
SMILES: | Brc1cc2NCCOc2cc1F |
Complexity: | 169 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 2.4 |
6-Bromo-7-fluoro-3,4-dihydro-2H-1,4-benzoxazine is a versatile compound that finds wide application in chemical synthesis. This compound serves as a key building block in the creation of various organic molecules, particularly in the pharmaceutical and agrochemical industries.One of the notable applications of 6-Bromo-7-fluoro-3,4-dihydro-2H-1,4-benzoxazine is its role as a precursor in the synthesis of heterocyclic compounds. By utilizing the unique reactivity of the bromo and fluoro substituents on the benzoxazine ring, chemists can introduce additional functional groups and manipulate the chemical structure to generate novel compounds with desired properties.Furthermore, the presence of both bromine and fluorine atoms in 6-Bromo-7-fluoro-3,4-dihydro-2H-1,4-benzoxazine enhances the compound's reactivity and allows for selective transformations during chemical reactions. This enables the synthesis of complex molecules with high efficiency and selectivity, making it a valuable tool in organic synthesis.Overall, 6-Bromo-7-fluoro-3,4-dihydro-2H-1,4-benzoxazine plays a crucial role in the development of various functional materials and bioactive compounds through its strategic incorporation into chemical synthesis strategies.