2,3-Dimethoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
95%
- Product Code: 40696
CAS:
1131335-62-0
Molecular Weight: | 265.1132 g./mol | Molecular Formula: | C₁₃H₂₀BNO₄ |
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EC Number: | MDL Number: | MFCD11857650 | |
Melting Point: | Boiling Point: | 353.2±42.0 ℃ at 760 mmHg | |
Density: | 1.09±0.1 g/cm3 | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the field of pharmaceuticals. Its boronate ester functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of drugs, agrochemicals, and organic materials. Additionally, its pyridine moiety contributes to its role in the development of ligands for catalysis, enhancing the efficiency of various chemical transformations. The compound’s stability and reactivity also make it suitable for use in the design of advanced materials, such as organic electronic components and polymers.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | £284.57 |
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0.250 | 10-20 days | £427.05 |
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2,3-Dimethoxy-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the field of pharmaceuticals. Its boronate ester functional group makes it a valuable reagent in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of drugs, agrochemicals, and organic materials. Additionally, its pyridine moiety contributes to its role in the development of ligands for catalysis, enhancing the efficiency of various chemical transformations. The compound’s stability and reactivity also make it suitable for use in the design of advanced materials, such as organic electronic components and polymers.
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