AG68112
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 98% | in stock | $7.00 | $5.00 | - + | |
5g | 98% | in stock | $11.00 | $8.00 | - + | |
10g | 98% | in stock | $18.00 | $13.00 | - + | |
25g | 98% | in stock | $42.00 | $30.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AG68112 |
Chemical Name: | 5-Bromo-2-iodoaniline |
CAS Number: | 64085-52-5 |
Molecular Formula: | C6H5BrIN |
Molecular Weight: | 297.9191 |
MDL Number: | MFCD09753734 |
SMILES: | Brc1ccc(c(c1)N)I |
Complexity: | 99.1 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 1 |
XLogP3: | 2.6 |
5-Bromo-2-iodoaniline, also known as 2-amino-5-bromoiodobenzene, serves as a versatile building block in chemical synthesis due to its unique structural features and reactivity. This compound is commonly employed in organic synthesis as a key intermediate for the preparation of various biologically active molecules and complex organic compounds. One significant application of 5-Bromo-2-iodoaniline is its use in the synthesis of pharmaceuticals and agrochemicals. Its incorporation into drug molecules can influence their biological activity, solubility, and pharmacokinetic properties. Additionally, the presence of both bromine and iodine functional groups in the molecule offers opportunities for diversification through further derivatization reactions.In addition, 5-Bromo-2-iodoaniline can participate in transition metal-catalyzed cross-coupling reactions to form carbon-carbon or carbon-heteroatom bonds. This enables the construction of more complex molecular structures, making it a valuable precursor in the synthesis of various organic materials, dyes, and functionalized intermediates.Furthermore, the unique electronic properties of 5-Bromo-2-iodoaniline make it a useful reagent in organic transformations such as electrophilic aromatic substitution and nucleophilic aromatic substitution reactions. These reactivity profiles allow for the straightforward introduction of the bromine and iodine functionalities into target molecules, enabling the modification and functionalization of aromatic systems.Overall, 5-Bromo-2-iodoaniline plays a crucial role in chemical synthesis, offering diverse synthetic pathways for the construction of complex organic molecules with potential applications in the pharmaceutical, agrochemical, and materials industries.