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CS-W001157 4
Total: USD 88.00

6-Bromo-1H-indazol-3-ol

  • CAS No. 885521-92-6

  • Cat. No. CS-W022448
  • Purity≥98%
  • MDL No.MFCD07781600

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

6-Bromo-1H-indazol-3-ol|CS-W022448

Structure of 885521-92-6

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General Information

  • CAS No. 885521-92-6
  • Cat. No. CS-W022448
  • Purity ≥98%
  • MDL No. MFCD07781600
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₇H₅BrN₂O
  • Molecular Weight 213.03
  • Synonym(s) 6-Bromo-1,2-dihydro-3H-indazol-3-one
  • SMILES BrC1=CC=C2C(=C1)[NH]N=C2O

Description

6-Bromo-1H-indazol-3-ol features a brominated indazolol scaffold with a phenolic hydroxyl group, offering enhanced reactivity for cross-coupling and functionalization. The electron-deficient heterocycle facilitates transition-metal catalyzed transformations, while the hydroxyl moiety enables hydrogen bonding and strategic derivatization. This bench-stable compound serves as a key intermediate in medicinal chemistry and materials synthesis.

Application

6-Bromo-1H-indazol-3-ol serves as a versatile building block for the synthesis of biologically active heterocycles, leveraging its bromine and phenolic hydroxyl groups for subsequent cross-coupling and functionalization. The molecule exhibits good bench stability and facilitates efficient derivatization via Pd-catalyzed reactions, enabling rapid access to substituted indazoles relevant in medicinal chemistry.

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   48.91
  • LogP   2.031
  • H_Acceptors   2
  • H_Donors   2
  • Rotatable_Bonds   0

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