tert-Butyl 5-bromo-6-methyl-1H-indazole-1-carboxylate

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Reagent Code: #150423
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CAS Number 1305320-67-5

science Other reagents with same CAS 1305320-67-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.17 g/mol
Formula C₁₃H₁₅BrN₂O₂
badge Registry Numbers
MDL Number MFCD16628189
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure allows for selective functionalization, making it valuable in developing drug candidates for cancer and inflammatory diseases. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura or Buchwald-Hartwig aminations to build complex indazole derivatives. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,880.00
inventory 250mg
10-20 days ฿3,120.00
inventory 1g
10-20 days ฿8,640.00

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tert-Butyl 5-bromo-6-methyl-1H-indazole-1-carboxylate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure allows for selective functionalization, making it valuable in developing drug candidates for cancer and inflammatory diseases. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura or Buchwald-Hartwig aminations to build complex indazole derivatives. Also utilized in agrochemical research for designing novel pesticides with improved e

Used as an intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research targeting kinase inhibitors. Its structure allows for selective functionalization, making it valuable in developing drug candidates for cancer and inflammatory diseases. Commonly employed in cross-coupling reactions such as Suzuki-Miyaura or Buchwald-Hartwig aminations to build complex indazole derivatives. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and selectivity.

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