4-Chloro-2-methoxybenzeneboronic acid

98%

Reagent Code: #90628
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CAS Number 762287-57-0

science Other reagents with same CAS 762287-57-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.4 g/mol
Formula C₇H₈BClO₃
badge Registry Numbers
MDL Number MFCD02684317
thermostat Physical Properties
Melting Point 128-134°C
inventory_2 Storage & Handling
Storage room temperature, cool

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active drug ingredients. Additionally, it is employed in material science for the synthesis of advanced polymers and electronic materials, where precise molecular architecture is required. Its stability and reactivity make it a valuable reagent in research and industrial applications.

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Test Parameter Specification
Purity (HPLC) 98-100
Melting Point (°C) 128-134
Carbon (Elemental Analysis) 43.6-45.5
Oxygen by Elemental Analysis 24.9-25.9
Appearance White to off-white powder or crystals

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿290.00
inventory 1g
10-20 days ฿560.00
inventory 5g
10-20 days ฿1,920.00
inventory 25g
10-20 days ฿8,420.00

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4-Chloro-2-methoxybenzeneboronic acid
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active drug ingredients. Additionally, it is employed in material science for the synthesis of advanced polymers and e

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for creating complex organic molecules, often in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many active drug ingredients. Additionally, it is employed in material science for the synthesis of advanced polymers and electronic materials, where precise molecular architecture is required. Its stability and reactivity make it a valuable reagent in research and industrial applications.

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