4-(N-Boc-amino)phenylboronic acid

97%

  • Product Code: 90479
  Alias:    4-(Boc-amino)phenylboronic acid
  CAS:    380430-49-9
Molecular Weight: 237.06 g./mol Molecular Formula: CH₃₃CO₂CNHC₆H₄BOH₂
EC Number: MDL Number: MFCD02093054
Melting Point: 199-204 °C (dec.)(lit.) Boiling Point:
Density: Storage Condition: 2~8°C
Product Description: Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, it serves as a key intermediate for creating biaryl compounds. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in pharmaceutical research for developing drug candidates. Additionally, the N-Boc protecting group ensures stability during reactions, allowing for selective deprotection when needed. This compound is also employed in the synthesis of complex molecules, including natural products and materials with potential applications in electronics and catalysis. Its versatility makes it a crucial tool in modern synthetic chemistry.
Product Specification:
Test Specification
Purity 97 100%
MELTING POINT 199-204
APPEARANCE COLOR White to Brown
APPEARANCE FORM Solid or Powder or Crystals or Chunks
PROTON NMR SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days €14.51
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5.000 10-20 days €38.25
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25.000 10-20 days €176.76
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4-(N-Boc-amino)phenylboronic acid
Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, it serves as a key intermediate for creating biaryl compounds. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in pharmaceutical research for developing drug candidates. Additionally, the N-Boc protecting group ensures stability during reactions, allowing for selective deprotection when needed. This compound is also employed in the synthesis of complex molecules, including natural products and materials with potential applications in electronics and catalysis. Its versatility makes it a crucial tool in modern synthetic chemistry.
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