AB44097
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 98% | in stock | $6.00 | $5.00 | - + | |
5g | 98% | in stock | $11.00 | $8.00 | - + | |
10g | 98% | in stock | $12.00 | $9.00 | - + | |
25g | 98% | in stock | $26.00 | $19.00 | - + | |
100g | 98% | in stock | $91.00 | $64.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB44097 |
Chemical Name: | 2-Amino-5-bromopyridin-3-ol |
CAS Number: | 39903-01-0 |
Molecular Formula: | C5H5BrN2O |
Molecular Weight: | 189.01 |
MDL Number: | MFCD09744143 |
SMILES: | Brc1cnc(c(c1)O)N |
Complexity: | 101 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 2 |
XLogP3: | 0.8 |
2-Amino-3-hydroxy-5-bromopyridine, a versatile chemical compound widely used in chemical synthesis, plays a crucial role in the production of various pharmaceuticals and agrochemicals. This compound serves as a key building block in the synthesis of complex organic molecules due to its unique structural properties and reactivity. In chemical synthesis, 2-Amino-3-hydroxy-5-bromopyridine is utilized as a precursor in the formation of heterocyclic compounds, which are essential components in the development of novel drugs and crop protection agents. Its functional groups enable it to participate in a wide range of synthetic reactions, including nucleophilic substitution, condensation, and oxidation processes.Furthermore, the presence of the bromine atom in 2-Amino-3-hydroxy-5-bromopyridine provides opportunities for further modifications through metal-catalyzed cross-coupling reactions, enabling the introduction of diverse functional groups into the molecule. This versatility allows for the creation of new chemical entities with enhanced biological activities and improved properties.Overall, 2-Amino-3-hydroxy-5-bromopyridine is a valuable intermediate in chemical synthesis, driving innovation in the fields of pharmaceuticals and agrochemicals through its contribution to the development of novel compounds with potential therapeutic and agricultural applications.
Acta crystallographica. Section E, Structure reports online 20110301