tert-butyl(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethyl)carbamate

98%

  • Product Code: 197463
  CAS:    1414475-01-6
Molecular Weight: 337.23 g./mol Molecular Formula: C₁₆H₂₈BN₃O₄
EC Number: MDL Number: MFCD28717087
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: Widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, this compound serves as a valuable intermediate for constructing complex molecules in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation, while the protected pyrazole and carbamate functionalities allow for selective transformations and further derivatization. Its structure supports the development of bioactive compounds, especially in drug discovery where pyrazole motifs are present in active pharmaceutical ingredients. The tert-butyl carbamate (Boc) group provides stability during synthesis and can be easily removed under mild acidic conditions, enabling stepwise assembly of multi-component systems.
Sizes / Availability / Pricing:
Size Availability Price Quantity
100mg 10-20 days ฿7,120.00
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-
250mg 10-20 days ฿12,110.00
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-
tert-butyl(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethyl)carbamate
Widely used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, this compound serves as a valuable intermediate for constructing complex molecules in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation, while the protected pyrazole and carbamate functionalities allow for selective transformations and further derivatization. Its structure supports the development of bioactive compounds, especially in drug discovery where pyrazole motifs are present in active pharmaceutical ingredients. The tert-butyl carbamate (Boc) group provides stability during synthesis and can be easily removed under mild acidic conditions, enabling stepwise assembly of multi-component systems.
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