tert-butyl-N-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl]carbamate
98%
Reagent
Code: #215143
CAS Number
1202794-01-1
blur_circular Chemical Specifications
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Molecular Information
Weight
283.1715 g/mol
Formula
C₁₄H₂₆BNO₄
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Registry Numbers
MDL Number
MFCD24466576
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Storage & Handling
Density
1.00±0.1 g/cm3(Predicted)
Storage
Room temperature
description 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.
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