AG23298
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 95% | in stock | $19.00 | $13.00 | - + | |
5g | 95% | in stock | $47.00 | $33.00 | - + | |
10g | 95% | in stock | $89.00 | $62.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AG23298 |
Chemical Name: | 2-Bromo-1-iodo-4-methoxybenzene |
CAS Number: | 466639-53-2 |
Molecular Formula: | C7H6BrIO |
Molecular Weight: | 312.9304 |
MDL Number: | MFCD12547848 |
SMILES: | COc1ccc(c(c1)Br)I |
Complexity: | 110 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 1 |
Rotatable Bond Count: | 1 |
XLogP3: | 3.2 |
2-Bromo-1-iodo-4-methoxybenzene, also known as BIBOMe, is a versatile chemical compound commonly used in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the creation of various organic compounds.One key application of 2-Bromo-1-iodo-4-methoxybenzene in chemical synthesis is as a precursor in the preparation of biaryl compounds. By undergoing cross-coupling reactions with different aryl or heteroaryl substrates, BIBOMe can be utilized to form complex biaryl structures with high efficiency and selectivity. This is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and materials with specific electronic properties.Furthermore, 2-Bromo-1-iodo-4-methoxybenzene can also participate in various other transformations, such as palladium-catalyzed C-N or C-O bond formations, Suzuki-Miyaura coupling reactions, and metal-catalyzed cross-coupling reactions. These synthetic routes enable the incorporation of the BIBOMe moiety into a wide range of organic scaffolds, facilitating the construction of diverse molecular architectures for further functionalization and applications in chemical research and industry.