tert-butyl (4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclohexyl)carbamate

98%

Reagent Code: #242152
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CAS Number 2694028-09-4

science Other reagents with same CAS 2694028-09-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 337.27 g/mol
Formula C₁₈H₃₂BNO₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used in organic synthesis as a protected amine-containing boronic ester derivative, enabling Suzuki-Miyaura cross-coupling reactions in the construction of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity at the boronic ester site. This compound is valuable for synthesizing functionalized amines and cyclic frameworks found in bioactive compounds. Its structure supports the development of drug candidates by facilitating carbon-carbon bond formation under mild palladium-catalyzed conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿2,510.00
100mg
10-20 days ฿17,460.00
500mg
10-20 days ฿52,380.00
1g
10-20 days ฿70,460.00
tert-butyl (4-((4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methylene)cyclohexyl)carbamate
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Used in organic synthesis as a protected amine-containing boronic ester derivative, enabling Suzuki-Miyaura cross-coupling reactions in the construction of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity at the boronic ester site. This compound is valuable for synthesizing functionalized amines and cyclic frameworks found in bioactive compounds. Its structure supports t
Used in organic synthesis as a protected amine-containing boronic ester derivative, enabling Suzuki-Miyaura cross-coupling reactions in the construction of complex organic molecules, particularly in pharmaceutical and agrochemical research. The tert-butyl carbamate group acts as a protecting group for the amine, allowing selective reactivity at the boronic ester site. This compound is valuable for synthesizing functionalized amines and cyclic frameworks found in bioactive compounds. Its structure supports the development of drug candidates by facilitating carbon-carbon bond formation under mild palladium-catalyzed conditions.
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