AA33685
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $14.00 | $10.00 | - + | |
1g | 97% | in stock | $16.00 | $11.00 | - + | |
10g | 97% | in stock | $28.00 | $20.00 | - + | |
500g | 97% | in stock | $1,350.00 | $945.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA33685 |
Chemical Name: | Methyl 5-bromo-2-hydroxynicotinate |
CAS Number: | 120034-05-1 |
Molecular Formula: | C7H6BrNO3 |
Molecular Weight: | 232.0314 |
MDL Number: | MFCD08056370 |
SMILES: | COC(=O)c1cc(Br)c[nH]c1=O |
Complexity: | 293 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 12 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Rotatable Bond Count: | 2 |
XLogP3: | 0.7 |
Methyl 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylate is a versatile compound widely utilized in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural properties. In chemical synthesis, Methyl 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylate acts as a key intermediate in the preparation of pharmaceuticals, agrochemicals, and fine chemicals. Its functional groups provide opportunities for further derivatization, allowing chemists to introduce diverse substituents and modify the compound for a range of applications. The presence of the bromo and ester groups in the molecule enables selective transformations through various chemical reactions such as nucleophilic substitution, Suzuki coupling, and Heck reactions. This flexibility in reactivity makes Methyl 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylate a valuable tool in organic synthesis, offering efficient routes to complex molecular structures.