tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate

≥95%

  • Product Code: 148633
  CAS:    1035235-26-7
Molecular Weight: 359.27 g./mol Molecular Formula: C₂₀H₃₀BNO₄
EC Number: MDL Number: MFCD11044677
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, stored in inert gas
Product Description: Widely used in cross-coupling reactions, especially in Suzuki-Miyaura coupling, this compound serves as a key intermediate in the synthesis of complex organic molecules, including pharmaceuticals and biologically active compounds. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. The protected dihydroisoquinoline scaffold allows for selective functionalization, which is particularly useful in constructing nitrogen-containing heterocycles found in many therapeutic agents. It is commonly employed in medicinal chemistry for building blocks and library synthesis in high-throughput screening programs.
Sizes / Availability / Pricing:
Size Availability Price Quantity
100mg 10-20 days ฿1,520.00
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250mg 10-20 days ฿3,370.00
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1g 10-20 days ฿7,960.00
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-
5g 10-20 days ฿34,580.00
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tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroisoquinoline-2(1H)-carboxylate
Widely used in cross-coupling reactions, especially in Suzuki-Miyaura coupling, this compound serves as a key intermediate in the synthesis of complex organic molecules, including pharmaceuticals and biologically active compounds. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development. The protected dihydroisoquinoline scaffold allows for selective functionalization, which is particularly useful in constructing nitrogen-containing heterocycles found in many therapeutic agents. It is commonly employed in medicinal chemistry for building blocks and library synthesis in high-throughput screening programs.
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