5-Chloro-2-methoxyphenylboronic acid

98%

Reagent Code: #90895
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Alias 5-Chloro-2-methoxyphenylboronic acid
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CAS Number 89694-48-4

science Other reagents with same CAS 89694-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.4 g/mol
Formula ClC₆H₃OCH₃BOH₂
badge Registry Numbers
MDL Number MFCD01318966
thermostat Physical Properties
Melting Point 134-141 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and diagnostic agents due to its ability to bind selectively with specific biological targets. Its stability and reactivity also make it a preferred choice in research and industrial applications for constructing carbon-carbon bonds in various chemical processes.

format_list_bulleted Product Specification

Test Parameter Specification
Melting point 134-141
Purity (HPLC) 98-100
Purity (Neutralization Titration) 97.5-103.5
Appearance White to light yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,580.00
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿580.00
inventory 100g
10-20 days ฿5,820.00

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5-Chloro-2-methoxyphenylboronic acid
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This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and diagnostic agents due to its ability to bind selectively with specific biological targets. Its

This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is utilized in the development of sensors and diagnostic agents due to its ability to bind selectively with specific biological targets. Its stability and reactivity also make it a preferred choice in research and industrial applications for constructing carbon-carbon bonds in various chemical processes.

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