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CS-W001157 4
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Ethyl 4-formyl-1H-pyrazole-3-carboxylate

  • CAS No. 179692-09-2

  • Cat. No. CS-0037733
  • Purity≥97%
  • MDL No.MFCD07643185

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

Ethyl 4-formyl-1H-pyrazole-3-carboxylate|CS-0037733

Structure of 179692-09-2

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General Information

  • CAS No. 179692-09-2
  • Cat. No. CS-0037733
  • Purity ≥97%
  • MDL No. MFCD07643185
  • Storage 4°C, stored under nitrogen
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₈N₂O₃
  • Molecular Weight 168.15
  • Synonym(s) Albb-007090
  • SMILES CCOC(=O)C1=NNC=C1C=O

Description

Ethyl 4-formyl-1H-pyrazole-3-carboxylate features a reactive aldehyde group flanked by electron-rich pyrazole and ester functionalities, enabling direct incorporation into diverse heterocyclic scaffolds. This bench-stable reagent integrates readily in multicomponent reactions and coupling processes, offering efficient access to functionalized pyrazole derivatives under standard conditions.

Application

Ethyl 4-formyl-1H-pyrazole-3-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrazole-based scaffolds through formyl group reactivity. The molecule combines a readily functionalized aldehyde with an ester handle, facilitating nucleophilic additions, condensations, and coupling reactions. Its bench-stable nature and compatibility with common reaction conditions make it well-suited for medicinal chemistry campaigns and process-scale applications.

Safety Information

Download SDS
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   72.05
  • LogP   0.3989
  • H_Acceptors   4
  • H_Donors   1
  • Rotatable_Bonds   3

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