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CS-W001157 4
Total: USD 88.00

4-Bromo-7-chloro-1H-indazole

  • CAS No. 1186334-61-1

  • Cat. No. CS-0050974
  • Purity≥97%
  • MDL No.None

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

4-Bromo-7-chloro-1H-indazole|CS-0050974

Structure of 1186334-61-1

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General Information

  • CAS No. 1186334-61-1
  • Cat. No. CS-0050974
  • Purity ≥97%
  • MDL No. None
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₄BrClN₂
  • Molecular Weight 231.48
  • Synonym(s) indazole,4-bromo-7-chloro
  • SMILES ClC1=CC=C(Br)C2=C1NN=C2

Description

4-Bromo-7-chloro-1H-indazole is a halogenated indazole scaffold featuring complementary reactive sites for cross-coupling and functionalization. The electron-deficient core enables efficient palladium-catalyzed transformations, while the bromine and chlorine substituents offer orthogonal reactivity. This compound serves as a key building block in medicinal chemistry and materials science.

Application

4-Bromo-7-chloro-1H-indazole serves as a versatile building block for the synthesis of biologically active heterocycles, enabling palladium-catalyzed cross-coupling reactions at both halogen sites. Its complementary reactivity profile facilitates sequential functionalization in medicinal chemistry and materials science. The molecule exhibits excellent bench stability, simplifies purification, and functions effectively in standard coupling protocols such as Suzuki-Miyaura and Stille reactions.

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   28.68
  • LogP   2.9788
  • H_Acceptors   1
  • H_Donors   1
  • Rotatable_Bonds   0

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