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AA00133

1000018-06-3 | 3-Amino-5-bromo-1-methyl-1h-indazole

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $18.00 $13.00 -   +
250mg 95% in stock $27.00 $19.00 -   +
1g 95% in stock $48.00 $34.00 -   +
5g 95% in stock $165.00 $116.00 -   +
100g 95% in stock $2,625.00 $1,837.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA00133
Chemical Name: 3-Amino-5-bromo-1-methyl-1h-indazole
CAS Number: 1000018-06-3
Molecular Formula: C8H8BrN3
Molecular Weight: 226.0732
MDL Number: MFCD09864804
SMILES: Brc1ccc2c(c1)c(N)nn2C

 

Computed Properties
Complexity: 176  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.9  

 

 

Upstream Synthesis Route
  • 5-Bromo-1-methyl-1H-indazol-3-amine, also known as $name$, is a versatile compound widely utilized in chemical synthesis as a key building block for the preparation of complex organic molecules. This compound exhibits valuable reactivity due to the bromine and amine functional groups present on the indazole ring.One of the primary applications of 5-Bromo-1-methyl-1H-indazol-3-amine in chemical synthesis is in the development of pharmaceutical compounds. By serving as a starting material, this compound can be further functionalized to introduce specific groups or motifs that are crucial for enhancing the biological activity or pharmacokinetic properties of the final drug molecule.Additionally, 5-Bromo-1-methyl-1H-indazol-3-amine can be employed in the synthesis of novel organic materials such as fluorescent dyes, agrochemicals, and ligands for catalysis. Its unique structure and reactivity make it a valuable substrate for diversification through various synthetic strategies, enabling the creation of a wide range of functionalized derivatives with tailored properties.Furthermore, this compound can also be utilized in the preparation of molecular probes and research tools for investigating biological processes or interactions. Its ability to undergo selective transformations under mild reaction conditions makes it a valuable asset for the design and development of specialized chemical probes aimed at studying specific targets in biochemical pathways.
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