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CS-W001157 4
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1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-amine

  • CAS No. 2172072-40-9

  • Cat. No. CS-0528800
  • Purity≥98%
  • MDL No.None

*For research and further manufacturing use only, not for direct human use.

1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-amine|CS-0528800

Structure of 2172072-40-9

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General Information

  • CAS No. 2172072-40-9
  • Cat. No. CS-0528800
  • Purity ≥98%
  • MDL No. None
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₈N₄
  • Molecular Weight 148.17
  • Synonym(s) None
  • SMILES NC1=CN=CC2=C1C=NN2C

Description

1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-amine features a fused heterocyclic core with a methylated pyrazole ring and an exocyclic amine, delivering enhanced electron density at the reaction site. This scaffold exhibits excellent bench stability and solubility in common organic solvents, enabling straightforward incorporation into medicinal chemistry campaigns. The compound serves as a key building block for kinase inhibitors and other bioactive small molecules.

Application

1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-amine serves as a versatile heterocyclic building block in medicinal chemistry, enabling rapid access to kinase inhibitor scaffolds. Its pyrazolopyridine core exhibits favorable bench stability and compatibility with standard coupling reactions. The pendant amine facilitates derivatization via acylation, alkylation, or Suzuki coupling, while the methyl group enhances metabolic stability and modulates electronic properties. Functions effectively in parallel synthesis campaigns and offers predictable reactivity in transition-metal-catalyzed transformations.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319
Precautionary Statements : P264-P280-P302+P352-P362

Quality Control

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Computational Chemistry Data

  • TPSA   56.73
  • LogP   0.5505
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   0

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