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CS-W001157 4
Total: USD 88.00

7-Bromo-1H-indazol-5-amine

  • CAS No. 953411-10-4

  • Cat. No. CS-W022524
  • Molecule weight212.05
  • Purity≥98%
  • MDL No.MFCD08275114

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

7-Bromo-1H-indazol-5-amine|CS-W022524

Structure of 953411-10-4

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General Information

  • CAS No. 953411-10-4
  • Cat. No. CS-W022524
  • Purity ≥98%
  • MDL No. MFCD08275114
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₆BrN₃
  • Molecular Weight 212.05
  • Synonym(s) 5-amino-7-bromo-1h-indazole
  • SMILES NC1=CC2=C(NN=C2)C(Br)=C1

Description

7-Bromo-1H-indazol-5-amine features a brominated indazole scaffold with a primary amine at the 5-position, enabling direct coupling in C–N cross-coupling reactions. The electron-deficient aromatic system enhances reactivity in transition-metal-catalyzed transformations, while the bench-stable, moisture-tolerant structure supports reliable handling in synthetic workflows.

Application

7-Bromo-1H-indazol-5-amine serves as a versatile building block in medicinal chemistry, enabling direct incorporation into biologically active scaffolds via palladium-catalyzed cross-coupling reactions. The bromo group facilitates efficient functionalization, while the primary amine supports derivatization through acylation, alkylation, or reductive amination. Its stability under standard reaction conditions and compatibility with diverse coupling partners make it a practical choice for constructing heterocyclic libraries and lead optimization campaigns.

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   54.7
  • LogP   1.9076
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   0

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