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tert-Butyl (6R)-6-methyl-4H,5H,6H,7H-pyrazolo[1,5-a]pyrazine-5-carboxylate

  • CAS No. 1639881-13-2

  • Cat. No. CS-0058080
  • Molecule weight237.30
  • Purity≥97%
  • MDL No.None

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

tert-Butyl (6R)-6-methyl-4H,5H,6H,7H-pyrazolo[1,5-a]pyrazine-5-carboxylate|CS-0058080

Structure of 1639881-13-2

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General Information

  • CAS No. 1639881-13-2
  • Cat. No. CS-0058080
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₉N₃O₂
  • Molecular Weight 237.30
  • Synonym(s) None
  • SMILES O=C(N1CC2=CC=NN2C[C@H]1C)OC(C)(C)C

Description

tert-Butyl (6R)-6-methyl-4H,5H,6H,7H-pyrazolo[1,5-a]pyrazine-5-carboxylate is a stereodefined heterocyclic building block featuring a chiral methyl group at the 6-position. This bench-stable derivative integrates seamlessly into synthetic routes requiring controlled stereochemistry and enhanced solubility in organic media. The tert-butyl ester facilitates straightforward deprotection under mild acidic conditions.

Application

tert-Butyl (6R)-6-methyl-4H,5H,6H,7H-pyrazolo[1,5-a]pyrazine-5-carboxylate serves as a stereochemically defined building block for the synthesis of pyrazolo[1,5-a]pyrazine scaffolds. Its tert-butyl ester group enables facile deprotection under mild acidic conditions, while the methyl substituent at the 6-position provides a key handle for further functionalization. The compound exhibits excellent bench stability and compatibility with standard coupling reactions, facilitating efficient access to diverse heterocyclic architectures in medicinal chemistry campaigns.

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-P330-P362+P364-P405-P501

Quality Control

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Computational Chemistry Data

  • TPSA   47.36
  • LogP   2.0223
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   0

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