(4-(1-((tert-Butoxycarbonyl)amino)cyclopropyl)phenyl)boronic acid

98%

Reagent Code: #89214
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CAS Number 1217500-58-7

science Other reagents with same CAS 1217500-58-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.12 g/mol
Formula C₁₄H₂₀BNO₄
badge Registry Numbers
MDL Number MFCD12546458
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during reactions, allowing for selective deprotection in multi-step synthesis processes. Its cyclopropyl group also contributes to unique steric and electronic properties, which can be exploited in the design of bioactive compounds or materials with specific functionalities.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿1,971.00
250mg
10-20 days ฿3,339.00
(4-(1-((tert-Butoxycarbonyl)amino)cyclopropyl)phenyl)boronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during reactions, allowing for selective deprotection in multi-step synthesis p

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The tert-butoxycarbonyl (Boc) protecting group enhances its stability during reactions, allowing for selective deprotection in multi-step synthesis processes. Its cyclopropyl group also contributes to unique steric and electronic properties, which can be exploited in the design of bioactive compounds or materials with specific functionalities.

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