2-((2'-Chloro-5'-(trifluoromethyl)phenoxy)methyl)phenylboronic acid(contains varying amounts of Anhydride)

95%

Reagent Code: #115565
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CAS Number 849062-11-9

science Other reagents with same CAS 849062-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 330.5 g/mol
Formula C₁₄H₁₁BClF₃O₃
badge Registry Numbers
MDL Number MFCD07369758
thermostat Physical Properties
Melting Point 138-147 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and advanced materials. Additionally, its trifluoromethyl and chloro substituents contribute to its role in the synthesis of compounds with enhanced biological activity and stability, making it useful in the design of drugs targeting specific diseases or pests. The presence of anhydride impurities does not significantly hinder its application in these processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,584.00
inventory 1g
10-20 days ฿4,455.00

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2-((2'-Chloro-5'-(trifluoromethyl)phenoxy)methyl)phenylboronic acid(contains varying amounts of Anhydride)
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This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and advanced materials. Additionally, its trifluoromethyl and chloro substituents contribute to

This chemical is primarily utilized as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in creating complex organic molecules, including active pharmaceutical ingredients (APIs) and advanced materials. Additionally, its trifluoromethyl and chloro substituents contribute to its role in the synthesis of compounds with enhanced biological activity and stability, making it useful in the design of drugs targeting specific diseases or pests. The presence of anhydride impurities does not significantly hinder its application in these processes.

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