2-[(3′,5′-Difluorophenoxy)methyl]phenylboronic acid(contains varying amounts of Anhydride)

95%

Reagent Code: #115994
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CAS Number 1218790-92-1

science Other reagents with same CAS 1218790-92-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 264.03 g/mol
Formula C₁₃H₁₁BF₂O₃
badge Registry Numbers
MDL Number MFCD11656035
thermostat Physical Properties
Melting Point 168-175 °C
inventory_2 Storage & Handling
Storage 2-8°C, stored in argon

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its difluorophenoxy moiety can enhance the metabolic stability and bioavailability of drug candidates, making it valuable in medicinal chemistry. The presence of anhydride may influence its reactivity, allowing for tailored modifications in synthetic routes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,446.00
inventory 5g
10-20 days ฿14,031.00

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2-[(3′,5′-Difluorophenoxy)methyl]phenylboronic acid(contains varying amounts of Anhydride)
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its difluorophenoxy moiety can enhance the metabolic stability and bioavailability of drug candidates,

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of pharmaceuticals, particularly in the development of drugs targeting specific biological pathways. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, its difluorophenoxy moiety can enhance the metabolic stability and bioavailability of drug candidates, making it valuable in medicinal chemistry. The presence of anhydride may influence its reactivity, allowing for tailored modifications in synthetic routes.

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