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tert-Butyl 7-bromo-1H-indazole-1-carboxylate

  • CAS No. 1092352-37-8

  • Cat. No. CS-0006107
  • Purity≥95%
  • MDL No.MFCD11505878

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

tert-Butyl 7-bromo-1H-indazole-1-carboxylate|CS-0006107

Structure of 1092352-37-8

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General Information

  • CAS No. 1092352-37-8
  • Cat. No. CS-0006107
  • Purity ≥95%
  • MDL No. MFCD11505878
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₃BrN₂O₂
  • Molecular Weight None
  • Synonym(s) 7-Bromoindazole-1-carboxylic acid tert-butyl ester
  • SMILES O=C(N1N=CC2=C1C(Br)=CC=C2)OC(C)(C)C

Description

tert-Butyl 7-bromo-1H-indazole-1-carboxylate features a brominated indazole core with a robust tert-butyl ester handle, enabling direct incorporation into cross-coupling reactions. The electron-deficient aromatic system facilitates palladium-catalyzed transformations, while the bench-stable protecting group simplifies purification and handling under standard conditions.

Application

tert-Butyl 7-bromo-1H-indazole-1-carboxylate serves as a versatile building block for the synthesis of brominated indazole derivatives, enabling efficient late-stage functionalization in medicinal chemistry and agrochemical research. The tert-butyl ester group offers excellent bench stability and facile removal under mild acidic conditions, while the bromine substituent provides a reliable handle for palladium-catalyzed cross-coupling reactions, including Suzuki, Stille, and Negishi transformations. Its compatibility with diverse reaction conditions makes it ideal for constructing complex heterocyclic scaffolds in high-purity formats.

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   44.12
  • LogP   3.582
  • H_Acceptors   4
  • H_Donors   0
  • Rotatable_Bonds   0

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