tert-butyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]carbamate

98%

  • Product Code: 215143
  CAS:    1202794-01-1
Molecular Weight: 283.1715 g./mol Molecular Formula: C₁₄H₂₆BNO₄
EC Number: MDL Number: MFCD24466576
Melting Point: Boiling Point:
Density: 1.00±0.1 g/cm3(Predicted) Storage Condition: Room temperature
Product Description: Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient carbon-carbon bond formation under mild conditions. Its allylic amine derivative protected by a tert-butoxycarbonyl (Boc) group makes it valuable for constructing nitrogen-containing heterocycles and bioactive compounds. The stability and reactivity profile support its use in multi-step syntheses where selective transformations are required.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.100 10-20 days Ft54,853.17
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0.250 10-20 days Ft78,601.87
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1.000 10-20 days Ft164,979.85
+
-
5.000 10-20 days Ft455,008.13
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tert-butyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]carbamate
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient carbon-carbon bond formation under mild conditions. Its allylic amine derivative protected by a tert-butoxycarbonyl (Boc) group makes it valuable for constructing nitrogen-containing heterocycles and bioactive compounds. The stability and reactivity profile support its use in multi-step syntheses where selective transformations are required.
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