tert-butyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]carbamate
98%
- Product Code: 215143
CAS:
1202794-01-1
Molecular Weight: | 283.1715 g./mol | Molecular Formula: | C₁₄H₂₆BNO₄ |
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EC Number: | MDL Number: | MFCD24466576 | |
Melting Point: | Boiling Point: | ||
Density: | 1.00±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient carbon-carbon bond formation under mild conditions. Its allylic amine derivative protected by a tert-butoxycarbonyl (Boc) group makes it valuable for constructing nitrogen-containing heterocycles and bioactive compounds. The stability and reactivity profile support its use in multi-step syntheses where selective transformations are required.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.100 | 10-20 days | Ft54,853.17 |
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0.250 | 10-20 days | Ft78,601.87 |
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1.000 | 10-20 days | Ft164,979.85 |
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5.000 | 10-20 days | Ft455,008.13 |
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tert-butyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]carbamate
Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. The boronate ester group enables Suzuki-Miyaura coupling, allowing efficient carbon-carbon bond formation under mild conditions. Its allylic amine derivative protected by a tert-butoxycarbonyl (Boc) group makes it valuable for constructing nitrogen-containing heterocycles and bioactive compounds. The stability and reactivity profile support its use in multi-step syntheses where selective transformations are required.
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