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2-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine

  • CAS No. 1511297-53-2

  • Cat. No. CS-0499259
  • Purity≥97%
  • MDL No.None

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

2-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine|CS-0499259

Structure of 1511297-53-2

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General Information

  • CAS No. 1511297-53-2
  • Cat. No. CS-0499259
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₆ClN₃
  • Molecular Weight 167.60
  • Synonym(s) None
  • SMILES CN1C=CC2=NC(Cl)=NC=C21

Description

2-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine features a fused heterocyclic core with a chlorine atom at the 2-position and a methyl group at the 5-position, providing a robust scaffold for nucleophilic substitution reactions. This electron-deficient pyrrolopyrimidine integrates readily into pharmaceutical intermediates and functional materials, offering high reactivity under standard conditions while maintaining bench stability.

Application

2-Chloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient construction of purine-derived scaffolds. Its chloro group at the C2 position facilitates nucleophilic substitution reactions, while the methyl substituent enhances metabolic stability and modulates electronic properties. The compound exhibits excellent bench stability and compatibility with standard coupling protocols, making it ideal for the synthesis of kinase inhibitors and other bioactive heterocycles.

Safety Information

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GHS Pictogram :
GHS No : GHS06
Signal Word : Danger
UN#: 2811
Class : 6.1
Packing Group : Ⅲ
Hazard Statements : H301-H311-H331
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P405-P501

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Computational Chemistry Data

  • TPSA   30.71
  • LogP   1.6217
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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