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CS-W001157 4
Total: USD 88.00

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid

  • CAS No. 1016241-80-7

  • Cat. No. CS-0018822
  • Purity≥97%
  • MDL No.MFCD11518907

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

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid|CS-0018822

Structure of 1016241-80-7

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General Information

  • CAS No. 1016241-80-7
  • Cat. No. CS-0018822
  • Purity ≥97%
  • MDL No. MFCD11518907
  • Storage -20°C, sealed storage, away from moisture
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄ClN₃O₂
  • Molecular Weight 197.58
  • Synonym(s) 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylicacid
  • SMILES O=C(C1=CC2=C(Cl)N=CN=C2N1)O

Description

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid features a fused heterocyclic core with a chlorine substituent at the 4-position and a carboxylic acid group at the 6-position. This combination enables direct incorporation into bioactive molecules, particularly in kinase inhibitor scaffolds and nucleoside analogues, where the electron-deficient pyrimidine ring enhances binding affinity. The compound exhibits stability under standard bench conditions and facilitates efficient derivatization via amide or ester formation.

Application

4-Chloro-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid serves as a versatile building block for purine-derived scaffolds in medicinal chemistry. Its ortho-chloro and carboxylic acid functionalities enable selective functionalization via palladium-catalyzed cross-coupling and amide formation. The compound exhibits bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis of kinase inhibitors and nucleoside analogs.

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   78.87
  • LogP   1.3095
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   1

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