N-Methyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
96%
- Product Code: 215716
CAS:
1036761-96-2
Molecular Weight: | 275.15 g./mol | Molecular Formula: | C₁₅H₂₂BNO₃ |
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EC Number: | MDL Number: | MFCD17015826 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials. The presence of the amide group allows for further derivatization or hydrogen bonding interactions, which can be exploited in drug design. Its stability and reactivity profile make it suitable for use in automated synthesis and library generation for high-throughput screening.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.100 | 10-20 days | Ft22,908.03 |
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0.250 | 10-20 days | Ft39,406.02 |
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1.000 | 10-20 days | Ft105,082.71 |
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N-Methyl-2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in the development of pharmaceuticals, agrochemicals, and functional materials. The presence of the amide group allows for further derivatization or hydrogen bonding interactions, which can be exploited in drug design. Its stability and reactivity profile make it suitable for use in automated synthesis and library generation for high-throughput screening.
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