2-Borono-1H-indol-1-carboxylic acid 1-Methyl ester

98%

  • Product Code: 39656
  CAS:    1001162-89-5
Molecular Weight: 219.0017 g./mol Molecular Formula: C₁₀H₁₀BNO₄
EC Number: MDL Number: MFCD22123264
Melting Point: Boiling Point:
Density: Storage Condition: -20℃, inert gas
Product Description: This compound is primarily utilized in organic synthesis, particularly in the development of boron-containing molecules. It serves as a key intermediate in the preparation of boron-based inhibitors and pharmaceuticals, especially those targeting proteases and kinases. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Additionally, it is explored in the design of enzyme inhibitors for therapeutic applications, such as cancer treatment, due to its ability to interact with biological targets. Its indole core structure also makes it relevant in the synthesis of bioactive compounds with potential applications in medicinal chemistry.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days £117.65
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1.000 10-20 days £353.57
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5.000 10-20 days £1,237.20
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2-Borono-1H-indol-1-carboxylic acid 1-Methyl ester
This compound is primarily utilized in organic synthesis, particularly in the development of boron-containing molecules. It serves as a key intermediate in the preparation of boron-based inhibitors and pharmaceuticals, especially those targeting proteases and kinases. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Additionally, it is explored in the design of enzyme inhibitors for therapeutic applications, such as cancer treatment, due to its ability to interact with biological targets. Its indole core structure also makes it relevant in the synthesis of bioactive compounds with potential applications in medicinal chemistry.
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