2-(tert-Butyldimethylsilyloxy)naphthalene-6-boronic acid
98%
- Product Code: 62355
CAS:
179942-45-1
Molecular Weight: | 302.25 g./mol | Molecular Formula: | C₁₆H₂₃BO₃Si |
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EC Number: | MDL Number: | MFCD04115644 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, in an inert gas |
Product Description:
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The tert-butyldimethylsilyloxy group provides stability and protects reactive sites during multi-step reactions, ensuring efficient and selective transformations. Additionally, it is employed in the development of organic electronic materials, such as OLEDs, due to its ability to form conjugated structures. Its versatility and reactivity make it a crucial tool in modern synthetic chemistry.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $90.61 |
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1.000 | 10-20 days | $281.73 |
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5.000 | 10-20 days | $954.21 |
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2-(tert-Butyldimethylsilyloxy)naphthalene-6-boronic acid
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. The tert-butyldimethylsilyloxy group provides stability and protects reactive sites during multi-step reactions, ensuring efficient and selective transformations. Additionally, it is employed in the development of organic electronic materials, such as OLEDs, due to its ability to form conjugated structures. Its versatility and reactivity make it a crucial tool in modern synthetic chemistry.
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