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Methyl 1H-pyrazolo[3,4-c]pyridine-5-carboxylate

  • CAS No. 1033772-26-7

  • Cat. No. CS-0049243
  • Purity≥97%
  • MDL No.None

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

Methyl 1H-pyrazolo[3,4-c]pyridine-5-carboxylate|CS-0049243

Structure of 1033772-26-7

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General Information

  • CAS No. 1033772-26-7
  • Cat. No. CS-0049243
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₇N₃O₂
  • Molecular Weight 177.16
  • Synonym(s) Methyl 1H-pyrazolo[3
  • SMILES COC(=O)C1=NC=C2NN=CC2=C1

Description

Methyl 1H-pyrazolo[3,4-c]pyridine-5-carboxylate is a heterocyclic ester featuring a fused pyrazolo[3,4-c]pyridine core with a strategically positioned methyl carboxylate group. This scaffold integrates readily into medicinal chemistry campaigns, offering a rigid, electron-deficient platform for targeted molecular design. The ester moiety enables further derivatization via hydrolysis or nucleophilic substitution, facilitating rapid access to diverse analogs. Bench-stable and moisture-tolerant, it supports efficient synthesis under standard conditions.

Application

Methyl 1H-pyrazolo[3,4-c]pyridine-5-carboxylate serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its pyrazolopyridine core exhibits robust bench stability and tolerates a range of functional groups, enabling straightforward derivatization via cross-coupling, nucleophilic substitution, or reduction. The ester moiety facilitates further transformations, including hydrolysis to the carboxylic acid or conversion to amides and other derivatives. This compound functions effectively in standard synthetic workflows requiring nitrogen-rich, planar scaffolds with predictable reactivity.

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 : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

  • TPSA   67.87
  • LogP   0.7445
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   1

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