tert-Butyl 3-bromo-1H-indazole-1-carboxylate

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Reagent Code: #45129
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CAS Number 1257296-40-4

science Other reagents with same CAS 1257296-40-4

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Weight 297.1600 g/mol
Formula C₁₂H₁₃BrN₂O₂
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MDL Number MFCD22380231
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various biologically active molecules, particularly in pharmaceutical research. It serves as a key building block in the development of indazole-based compounds, which are known for their potential therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. The tert-butyl group provides steric protection, enhancing the stability of the molecule during chemical transformations, while the bromo substituent allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Its application is particularly significant in the design and synthesis of drug candidates targeting specific enzymes or receptors in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,420.00

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tert-Butyl 3-bromo-1H-indazole-1-carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various biologically active molecules, particularly in pharmaceutical research. It serves as a key building block in the development of indazole-based compounds, which are known for their potential therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. The tert-butyl group provides steric protection, enhancing the stability of the molecule during chemical tra

This compound is primarily utilized in organic synthesis as a versatile intermediate for the preparation of various biologically active molecules, particularly in pharmaceutical research. It serves as a key building block in the development of indazole-based compounds, which are known for their potential therapeutic properties, including anti-inflammatory, anticancer, and antimicrobial activities. The tert-butyl group provides steric protection, enhancing the stability of the molecule during chemical transformations, while the bromo substituent allows for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings. Its application is particularly significant in the design and synthesis of drug candidates targeting specific enzymes or receptors in medicinal chemistry.

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