(4-(1-((tert-Butoxycarbonyl)(4-methoxybenzyl) amino)ethyl)phenyl)boronic acid

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Reagent Code: #89213
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CAS Number 1704096-66-1

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blur_circular Chemical Specifications

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Weight 385.26 g/mol
Formula C₂₁H₂₈BNO₅
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. Its boronic acid group makes it a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) and 4-methoxybenzyl (PMB) protecting groups enhance its stability during synthesis, allowing selective deprotection when needed. It is also utilized in the development of bioactive compounds, where its structure can be tailored to target specific biological pathways. Additionally, it serves as a building block in the synthesis of advanced materials, such as polymers and ligands for catalysis.

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inventory 1g
10-20 days ฿50,210.00
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(4-(1-((tert-Butoxycarbonyl)(4-methoxybenzyl) amino)ethyl)phenyl)boronic acid
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This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. Its boronic acid group makes it a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) and 4-methoxybenzyl (PMB) protecting groups enhance its stability during synthesis, allowing selective deprotection when needed. It is also utilized in the development

This chemical is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds. Its boronic acid group makes it a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The tert-butoxycarbonyl (Boc) and 4-methoxybenzyl (PMB) protecting groups enhance its stability during synthesis, allowing selective deprotection when needed. It is also utilized in the development of bioactive compounds, where its structure can be tailored to target specific biological pathways. Additionally, it serves as a building block in the synthesis of advanced materials, such as polymers and ligands for catalysis.

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