tert-Butyl(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)allyl)carbamate
97%
Reagent
Code: #155259
CAS Number
1374106-06-5
blur_circular Chemical Specifications
scatter_plot
Molecular Information
Weight
283.17 g/mol
Formula
C₁₄H₂₆BNO₄
badge
Registry Numbers
MDL Number
MFCD10698517
inventory_2
Storage & Handling
Storage
Room temperature
description Product Description
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. The allylic amine moiety protected by the tert-butoxycarbonyl (Boc) group allows for selective formation of carbon-carbon bonds in the synthesis of complex molecules, especially in pharmaceutical and agrochemical research. The Boc group can be easily removed under mild acidic conditions after coupling, enabling further functionalization of the amine. Its stability and reactivity profile make it valuable for constructing allylated aromatic or heteroaromatic systems in drug discovery and materials science.
shopping_cart Available Sizes & Pricing
Cart
No products
Subtotal:
0.00
Total
0.00
THB