4,4,5,5-Tetramethyl-2-(1-naphthyl)-1,3,2-dioxaborolane

≥98%

  • Product Code: 90299
  CAS:    68716-52-9
Molecular Weight: 254.14 g./mol Molecular Formula: C₁₆H₁₉BO₂
EC Number: MDL Number: MFCD05663869
Melting Point: 55-59°C Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for introducing the naphthyl group into various organic compounds, enabling the formation of carbon-carbon bonds. Its stability and reactivity make it a valuable tool in the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the preparation of boron-containing compounds for applications in materials science and optoelectronics. Its role in facilitating precise and efficient transformations highlights its importance in modern synthetic chemistry.
Product Specification:
Test Specification
Appearance White to almost white to yellow solid
Purity 97.5-100
Melting Point 55-59
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size Availability Price Quantity
200mg 10-20 days $21.27
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1g 10-20 days $42.01
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5g 10-20 days $158.47
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-
25g 10-20 days $381.83
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4,4,5,5-Tetramethyl-2-(1-naphthyl)-1,3,2-dioxaborolane
This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for introducing the naphthyl group into various organic compounds, enabling the formation of carbon-carbon bonds. Its stability and reactivity make it a valuable tool in the synthesis of complex molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the preparation of boron-containing compounds for applications in materials science and optoelectronics. Its role in facilitating precise and efficient transformations highlights its importance in modern synthetic chemistry.
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