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Home  > 1-(2-aminophenyl)-1H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one

AV28807

1087784-31-3 | 1-(2-aminophenyl)-1H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $139.00 $97.00 -   +
250mg 95% in stock $251.00 $176.00 -   +
1g 95% in stock $573.00 $402.00 -   +
5g 95% in stock $1,693.00 $1,185.00 -   +
10g 95% in stock $2,532.00 $1,772.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AV28807
Chemical Name: 1-(2-aminophenyl)-1H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one
CAS Number: 1087784-31-3
Molecular Formula: C11H9N5O
Molecular Weight: 227.2221
MDL Number: MFCD11099478
SMILES: Nc1ccccc1n1ncc2c1nc[nH]c2=O

 

Upstream Synthesis Route
  • 1-(2-Aminophenyl)-1H,4H,5H-pyrazolo[3,4-d]pyrimidin-4-one is a versatile compound that plays a crucial role in chemical synthesis by serving as a key building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows it to participate in a wide range of reactions, making it a valuable tool for organic chemists seeking to design and produce new molecules with desired properties. In particular, this compound is known for its ability to undergo functional group transformations, cyclization reactions, and substitution reactions, enabling the synthesis of diverse molecular architectures with potential biological and industrial applications. Its utility in chemical synthesis lies in its capacity to act as a scaffold for molecular modification, providing a platform for the construction of complex structures with specific functionalities. This compound's strategic placement of functional groups and its intrinsic reactivity make it a valuable component in the toolkit of synthetic chemists aiming to access novel compounds for various purposes.
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