5-(Ethoxycarbonyl)-2-fluorobenzeneboronic Acid (contains varying amounts of Anhydride)

95%

Reagent Code: #183084
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CAS Number 874219-60-0

science Other reagents with same CAS 874219-60-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.98 g/mol
Formula C₉H₁₀BFO₄
badge Registry Numbers
MDL Number MFCD08235094
thermostat Physical Properties
Melting Point 99°C
inventory_2 Storage & Handling
Storage Room temperature, 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 fluorinated biaryl compounds, which are important structural motifs in drug discovery due to their enhanced metabolic stability and bioavailability. The presence of the ethoxycarbonyl group allows for further functionalization or serves as a directing group in subsequent transformations. Often utilized in research and development of active pharmaceutical ingredients (APIs) where fluorinated aromatic systems are required. The product may contain varying amounts of anhydride, which enhances stability for storage and transportation.

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inventory 50mg
10-20 days ฿340.00

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5-(Ethoxycarbonyl)-2-fluorobenzeneboronic Acid (contains varying amounts of Anhydride)
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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 fluorinated biaryl compounds, which are important structural motifs in drug discovery due to their enhanced metabolic stability and bioavailability. The presence of the ethoxycarbonyl group

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 fluorinated biaryl compounds, which are important structural motifs in drug discovery due to their enhanced metabolic stability and bioavailability. The presence of the ethoxycarbonyl group allows for further functionalization or serves as a directing group in subsequent transformations. Often utilized in research and development of active pharmaceutical ingredients (APIs) where fluorinated aromatic systems are required. The product may contain varying amounts of anhydride, which enhances stability for storage and transportation.

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