2-(2-BROMOETHYL)BENZENEBORONIC ACID,PINACOL ESTER

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Reagent Code: #154655
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CAS Number 850567-53-2

science Other reagents with same CAS 850567-53-2

blur_circular Chemical Specifications

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Weight 311.02 g/mol
Formula C₁₄H₂₀BBrO₂
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its stability and reactivity make it suitable for constructing biaryl compounds and functionalized aromatic systems. Commonly employed in late-stage functionalization of complex molecules due to the tolerance of various functional groups. The ortho-bromoethyl substituent provides opportunities for additional synthetic transformations, such as nucleophilic substitutions, alkylations, or further cross-coupling reactions, allowing access to more intricate molecular scaffolds. Also utilized in materials science for synthesizing conjugated polymers and organic electronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,310.00
inventory 1g
10-20 days ฿33,920.00

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2-(2-BROMOETHYL)BENZENEBORONIC ACID,PINACOL ESTER
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Used in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its stability and reactivity make it suitable for constructing biaryl compounds and functionalized aromatic systems. Commonly employed in late-stage functionalization of complex molecules due to the tolerance of various functional groups. The ortho-bromoethyl substituent provides opportunities for additional synthet

Used in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its stability and reactivity make it suitable for constructing biaryl compounds and functionalized aromatic systems. Commonly employed in late-stage functionalization of complex molecules due to the tolerance of various functional groups. The ortho-bromoethyl substituent provides opportunities for additional synthetic transformations, such as nucleophilic substitutions, alkylations, or further cross-coupling reactions, allowing access to more intricate molecular scaffolds. Also utilized in materials science for synthesizing conjugated polymers and organic electronic materials.

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