[4-Chloro-2-(ethoxycarbonyl)phenyl]boronic acid

95%

Reagent Code: #162330
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CAS Number 850568-61-5

science Other reagents with same CAS 850568-61-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.4373 g/mol
Formula C₉H₁₀BClO₄
badge Registry Numbers
MDL Number MFCD06659823
thermostat Physical Properties
Melting Point 132-134 °C
Boiling Point 397.799 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.339 g/cm3
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl compounds, which are structural motifs in active pharmaceutical ingredients. The ester group allows for further functionalization, enhancing its utility in multi-step syntheses. Stable and compatible with a variety of reaction conditions, making it suitable for library synthesis in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,120.00
inventory 1g
10-20 days ฿10,930.00

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[4-Chloro-2-(ethoxycarbonyl)phenyl]boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl compounds, which are structural motifs in active pharmaceutical ingredients. The ester group allows for further functionalization, enhancing its utility in multi-step syntheses. Stabl

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronic acid functionality enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the preparation of biaryl compounds, which are structural motifs in active pharmaceutical ingredients. The ester group allows for further functionalization, enhancing its utility in multi-step syntheses. Stable and compatible with a variety of reaction conditions, making it suitable for library synthesis in drug discovery.

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