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Home  > Chemistry  > Heterocyclic Building Blocks  > Other Aromatic Heterocycles  > 6-Chloro-1-methyl-1H-pyrazolo[3,4-b]pyridin-3-amine

AD68035

1076197-93-7 | 6-Chloro-1-methyl-1H-pyrazolo[3,4-b]pyridin-3-amine

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $153.00 $107.00 -   +
1g 95% in stock $362.00 $254.00 -   +
5g 95% in stock $1,053.00 $737.00 -   +
10g 95% in stock $1,535.00 $1,074.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AD68035
Chemical Name: 6-Chloro-1-methyl-1H-pyrazolo[3,4-b]pyridin-3-amine
CAS Number: 1076197-93-7
Molecular Formula: C7H7ClN4
Molecular Weight: 182.6103
MDL Number: MFCD11109857
SMILES: Clc1ccc2c(n1)n(C)nc2N

 

Computed Properties
Complexity: 177  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.4  

 

 

Upstream Synthesis Route
  • As a professional chemist, I understand the significant role of 6-Chloro-1-methyl-1H-pyrazolo[3,4-b]pyridin-3-amine in chemical synthesis. This compound serves as a crucial building block in the creation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it an essential intermediate in the synthesis of complex organic molecules.Due to its specific chemical properties, 6-Chloro-1-methyl-1H-pyrazolo[3,4-b]pyridin-3-amine can participate in diverse chemical reactions such as nucleophilic substitution, coupling reactions, and palladium-catalyzed cross-coupling reactions. It can be used to introduce the chloro and methyl groups into target molecules, allowing for the synthesis of novel compounds with tailored functions and properties.Furthermore, the presence of the pyrazole and pyridine rings in this compound enables it to interact with biological receptors and enzymes, making it a valuable scaffold for designing biologically active molecules. By incorporating 6-Chloro-1-methyl-1H-pyrazolo[3,4-b]pyridin-3-amine into synthetic pathways, chemists can access a wide range of structurally diverse compounds with potential therapeutic or agricultural applications.
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