tert-Butyl 3-formyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate

98%

  • Product Code: 118187
  CAS:    1025707-92-9
Molecular Weight: 371.24 g./mol Molecular Formula: C₂₀H₂₆BNO₅
EC Number: MDL Number: MFCD07364063
Melting Point: Boiling Point:
Density: Storage Condition: -20°C, inert gas
Product Description: This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules, especially those involving indole derivatives. The presence of the formyl group and the boronate ester moiety makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, its tert-butyl carboxylate group provides stability and facilitates selective deprotection in multi-step synthetic processes. This chemical is also employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its versatility in functional group transformations makes it a valuable tool in medicinal chemistry and material science research.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $59.14
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0.250 10-20 days $100.18
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1.000 10-20 days $270.03
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tert-Butyl 3-formyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-1-carboxylate
This compound is primarily used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the construction of complex molecules, especially those involving indole derivatives. The presence of the formyl group and the boronate ester moiety makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. Additionally, its tert-butyl carboxylate group provides stability and facilitates selective deprotection in multi-step synthetic processes. This chemical is also employed in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its versatility in functional group transformations makes it a valuable tool in medicinal chemistry and material science research.
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