3-Methoxyphenylboronic acid

97%

Reagent Code: #90251
label
Alias 3-methoxyphenylboronic acid; 3-methoxyphenylboronic acid, m-methoxyphenylboronic acid
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CAS Number 10365-98-7

science Other reagents with same CAS 10365-98-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.96 g/mol
Formula C₇H₉BO₃
badge Registry Numbers
MDL Number MFCD00161359
thermostat Physical Properties
Melting Point 160-163 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It is also employed in the preparation of complex molecules for drug discovery, aiding in the development of potential therapeutic agents. Additionally, it serves as a building block in material science for creating advanced polymers and organic electronic materials. Its boronic acid group enables selective binding to diols, making it useful in carbohydrate sensing and biochemical research.

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Test Parameter Specification
Purity 97-100%
Melting point 160-162
Appearance White to light yellow powder

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿260.00
inventory 5g
10-20 days ฿410.00
inventory 25g
10-20 days ฿960.00
inventory 100g
10-20 days ฿3,200.00

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3-Methoxyphenylboronic acid
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It is also employed in the preparation of complex molecules for drug discovery, aiding in the development of potential therapeutic agents. Additionally, it serves as a building block in material science for creating advanced polymers and organic electronic materials. Its boronic acid group enables selective binding to

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds, which are essential in pharmaceuticals and agrochemicals. It is also employed in the preparation of complex molecules for drug discovery, aiding in the development of potential therapeutic agents. Additionally, it serves as a building block in material science for creating advanced polymers and organic electronic materials. Its boronic acid group enables selective binding to diols, making it useful in carbohydrate sensing and biochemical research.

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