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CS-W001157 4
Total: USD 88.00

7-Chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine

  • CAS No. 923282-39-7

  • Cat. No. CS-W009037
  • Purity≥98%
  • MDL No.MFCD10000618

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

7-Chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine|CS-W009037

Structure of 923282-39-7

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General Information

  • CAS No. 923282-39-7
  • Cat. No. CS-W009037
  • Purity ≥98%
  • MDL No. MFCD10000618
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₅ClN₄
  • Molecular Weight 168.58
  • Synonym(s) 7-chloro-1-methylpyrazolo[4,3-d]pyrimidine
  • SMILES CN1N=CC2=NC=NC(Cl)=C21

Description

7-Chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine is a bench-stable heterocyclic scaffold featuring a chlorinated pyrazolopyrimidine core. This electron-deficient system enables efficient coupling in transition-metal-catalyzed reactions and serves as a key building block in medicinal chemistry for kinase inhibitors and nucleoside analogs.

Application

7-Chloro-1-methyl-1H-pyrazolo[4,3-d]pyrimidine serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its electron-deficient pyrazolopyrimidine core enables efficient palladium-catalyzed cross-coupling reactions, while the 7-chloro and 1-methyl groups provide orthogonal functional handles for further derivatization. The compound exhibits excellent bench stability and facilitates rapid access to diverse scaffolds in drug discovery campaigns.

Synthesis

  • Route1

    References

    • Sunesis Pharmaceuticals, Inc. Patent: US2007/27166 A1, 2007 ; Location in patent: Page/Page column 80 ; US 20070027166 A1

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   43.6
  • LogP   1.0167
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   0

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