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CS-W001157 4
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3-Bromo-8-chloro-1,7-naphthyridine

  • CAS No. 1260670-05-0

  • Cat. No. CS-0051445
  • Molecule weight243.49
  • Purity≥97%
  • MDL No.None

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

3-Bromo-8-chloro-1,7-naphthyridine|CS-0051445

Structure of 1260670-05-0

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General Information

  • CAS No. 1260670-05-0
  • Cat. No. CS-0051445
  • Purity ≥97%
  • MDL No. None
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₄BrClN₂
  • Molecular Weight 243.49
  • Synonym(s) 3-BroMo-8-chloro-[1,7]naphthyridine
  • SMILES ClC1=NC=CC2=CC(Br)=CN=C12

Description

3-Bromo-8-chloro-1,7-naphthyridine features a dual halogenated naphthyridine core with orthogonal reactivity at the 3-bromo and 8-chloro positions. This electron-deficient scaffold enables selective cross-coupling transformations under palladium catalysis, facilitating rapid access to functionalized heterocyclic architectures in medicinal chemistry and materials science applications.

Application

3-Bromo-8-chloro-1,7-naphthyridine serves as a versatile building block in medicinal chemistry and materials science, enabling palladium-catalyzed cross-coupling reactions due to its dual halogen functionality. The bromo group offers high reactivity in Suzuki, Stille, and Negishi couplings, while the chloro substituent provides orthogonal reactivity for sequential functionalization. Bench-stable and readily purified by column chromatography, it facilitates efficient synthesis of complex heterocyclic scaffolds and advanced API intermediates.

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   25.78
  • LogP   3.0457
  • H_Acceptors   2
  • H_Donors   0
  • Rotatable_Bonds   0

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