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Home  > 7-Amino-4-bromo-1h-indazole

AA22952

1190319-80-2 | 7-Amino-4-bromo-1h-indazole

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 1 week $219.00 $153.00 -   +
100mg 95% 1 week $284.00 $199.00 -   +
250mg 95% 1 week $371.00 $260.00 -   +
500mg 95% 1 week $535.00 $375.00 -   +
1g 95% 1 week $663.00 $464.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA22952
Chemical Name: 7-Amino-4-bromo-1h-indazole
CAS Number: 1190319-80-2
Molecular Formula: C7H6BrN3
Molecular Weight: 212.0466
MDL Number: MFCD12963529
SMILES: Brc1ccc(c2c1cn[nH]2)N

 

Upstream Synthesis Route
  • $Name$ is a versatile chemical compound that finds widespread application in chemical synthesis. One of its primary uses is as a building block in the preparation of various bioactive molecules and pharmaceutical intermediates. By incorporating $name$ into synthetic routes, chemists can access a diverse array of functionalized compounds that exhibit potential therapeutic properties.In particular, 4-Bromo-1H-indazol-7-amine serves as a valuable precursor in the synthesis of heterocyclic compounds and complex organic structures. Its unique chemical properties enable it to participate in a range of important reactions, including Suzuki coupling, Buchwald-Hartwig amination, and cross-coupling reactions. These synthetic transformations allow for the efficient construction of novel molecules with potential applications in drug discovery and material science.Moreover, the presence of the bromo group in $name$ provides a handle for further functionalization, enabling the introduction of additional substituents or modification of the core structure. This flexibility is crucial for fine-tuning the properties of the synthesized compounds and optimizing their biological activities.Overall, the strategic incorporation of 4-Bromo-1H-indazol-7-amine in chemical synthesis offers chemists a powerful tool for accessing diverse molecular architectures and expanding the scope of organic chemistry research.
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