N-((Tetrahydrofuran-2-yl)methyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

97%

  • Product Code: 58915
  CAS:    1073355-09-5
Molecular Weight: 331.21 g./mol Molecular Formula: C₁₈H₂₆BNO₄
EC Number: MDL Number: MFCD09266200
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic ester reagent. Its structure, featuring a tetrahydrofuran group and a benzamide moiety, makes it valuable for constructing complex molecules, especially in pharmaceutical and agrochemical research. The boronic ester functionality enables the formation of carbon-carbon bonds, facilitating the synthesis of biaryl compounds, which are common in drug development. Additionally, its stability and reactivity under mild conditions make it a preferred choice for designing and producing novel organic compounds with potential therapeutic applications.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿1,890.00
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1.000 10-20 days ฿5,103.00
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5.000 10-20 days ฿17,856.00
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N-((Tetrahydrofuran-2-yl)methyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction, where it acts as a boronic ester reagent. Its structure, featuring a tetrahydrofuran group and a benzamide moiety, makes it valuable for constructing complex molecules, especially in pharmaceutical and agrochemical research. The boronic ester functionality enables the formation of carbon-carbon bonds, facilitating the synthesis of biaryl compounds, which are common in drug development. Additionally, its stability and reactivity under mild conditions make it a preferred choice for designing and producing novel organic compounds with potential therapeutic applications.
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