AB64279
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $8.00 | $5.00 | - + | |
1g | 97% | in stock | $13.00 | $9.00 | - + | |
5g | 97% | in stock | $20.00 | $14.00 | - + | |
10g | 97% | in stock | $29.00 | $20.00 | - + | |
25g | 97% | in stock | $62.00 | $43.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB64279 |
Chemical Name: | 3-Amino-6-bromo-1H-indazole |
CAS Number: | 404827-77-6 |
Molecular Formula: | C7H6BrN3 |
Molecular Weight: | 212.0466 |
MDL Number: | MFCD05665872 |
SMILES: | Brc1ccc2c(c1)[nH]nc2N |
Complexity: | 153 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 11 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
XLogP3: | 1.9 |
6-Bromo-1H-indazol-3-amine is a versatile compound commonly utilized in chemical synthesis for the development of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it a valuable building block in organic chemistry.In chemical synthesis, 6-Bromo-1H-indazol-3-amine serves as a key intermediate in the preparation of novel indazole derivatives with diverse biological activities. Its bromo functional group provides a site for further derivatization through cross-coupling reactions, allowing for the introduction of various substituents to tailor the molecule's properties.Furthermore, 6-Bromo-1H-indazol-3-amine can participate in transition metal-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig reactions, enabling the formation of complex molecular frameworks. This compound's versatility and synthetic utility make it a valuable tool for medicinal chemists and researchers working in the field of drug discovery.Overall, the application of 6-Bromo-1H-indazol-3-amine in chemical synthesis offers a strategic approach to accessing a wide range of structurally diverse compounds with potential biological activities, making it a valuable asset in modern organic chemistry research.