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CS-W001157 4
Total: USD 88.00

4-Chloro-6-iodothieno[2,3-d]pyrimidine

  • CAS No. 552295-08-6

  • Cat. No. CS-W000109
  • Purity≥98%
  • MDL No.MFCD09746333

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

4-Chloro-6-iodothieno[2,3-d]pyrimidine|CS-W000109

Structure of 552295-08-6

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General Information

  • CAS No. 552295-08-6
  • Cat. No. CS-W000109
  • Purity ≥98%
  • MDL No. MFCD09746333
  • Storage -20°C, sealed storage, away from moisture and light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₆H₂ClIN₂S
  • Molecular Weight 296.52
  • Synonym(s) 4-CHLORO-6-IODO-THIENO[2,3-D]PYRIMIDINE
  • SMILES ClC1=C(C2=NC=N1)C=C(S2)I

Description

4-Chloro-6-iodothieno[2,3-d]pyrimidine features a fused thienopyrimidine core with orthogonal halogen substituents enabling selective cross-coupling. The chlorine and iodine positions facilitate sequential functionalization in transition-metal-catalyzed reactions, offering precise control over molecular architecture. This scaffold delivers high reactivity under standard conditions while maintaining bench stability.

Application

4-Chloro-6-iodothieno[2,3-d]pyrimidine serves as a versatile building block for constructing bioactive heterocycles, enabling palladium-catalyzed cross-coupling reactions with high efficiency. The molecule’s complementary halogen functionality—chlorine at C4 and iodine at C6—facilitates sequential functionalization, while its thienopyrimidine core provides structural rigidity and favorable electronic properties for medicinal chemistry applications. Bench-stable and readily purified by crystallization, it is well-suited for scalable synthesis of kinase inhibitors and other pharmaceutical scaffolds.

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   25.78
  • LogP   2.9493
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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