4-Chloro-3-(methoxycarbonyl)phenylboronic acid

98%

Reagent Code: #90637
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CAS Number 874219-45-1

science Other reagents with same CAS 874219-45-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.41 g/mol
Formula C₈H₈BClO₄
badge Registry Numbers
MDL Number MFCD06801690
thermostat Physical Properties
Melting Point 136-138°C
Boiling Point 384.2°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used extensively in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for synthesizing biaryl compounds, which are crucial in pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Additionally, it is employed in the development of organic electronic materials, contributing to advancements in OLEDs and other optoelectronic devices. The methoxycarbonyl group enhances its stability and reactivity, making it a versatile reagent in organic synthesis.

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Test Parameter Specification
APPEARANCE WHITE TO PALE YELLOW SOLID
Purity 97.5-100
Melting Point 135-140

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿820.00
inventory 1g
10-20 days ฿2,150.00
inventory 5g
10-20 days ฿7,500.00

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4-Chloro-3-(methoxycarbonyl)phenylboronic acid
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Used extensively in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for synthesizing biaryl compounds, which are crucial in pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Additionally, it is employed in the development of organic electronic materials, contributing to advancements in OLEDs and other optoelectronic devices. The methoxycarbonyl group enhances its
Used extensively in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for synthesizing biaryl compounds, which are crucial in pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, enabling the creation of complex organic molecules. Additionally, it is employed in the development of organic electronic materials, contributing to advancements in OLEDs and other optoelectronic devices. The methoxycarbonyl group enhances its stability and reactivity, making it a versatile reagent in organic synthesis.
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