3-Ethoxy-5-fluorobenzeneboronic Acid (contains varying amounts of Anhydride)

95%

Reagent Code: #183083
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CAS Number 850589-53-6

science Other reagents with same CAS 850589-53-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.97 g/mol
Formula C₈H₁₀BFO₃
badge Registry Numbers
MDL Number MFCD07363779
thermostat Physical Properties
Melting Point 158°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, making it valuable in drug discovery and development. Commonly employed in the preparation of fluorinated biaryl compounds, which are important structural motifs in bioactive molecules due to enhanced metabolic stability and membrane permeability. Also utilized in materials science for constructing functional organic frameworks and conjugated systems.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿360.00
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3-Ethoxy-5-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, making it valuable in drug discovery and development. Commonly employed in the preparation of fluorinated biaryl compounds, which are important structural motifs in bioactive molecules due to enhanced metabolic stability and membr

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, making it valuable in drug discovery and development. Commonly employed in the preparation of fluorinated biaryl compounds, which are important structural motifs in bioactive molecules due to enhanced metabolic stability and membrane permeability. Also utilized in materials science for constructing functional organic frameworks and conjugated systems.

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