4-(Methanesulfonyl)phenylboronic acid

98%

Reagent Code: #90700
label
Alias 4-Methanesulfonylphenylboronic acid 4-Methylsulfonyl phenylboronic acid
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CAS Number 149104-88-1

science Other reagents with same CAS 149104-88-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.02 g/mol
Formula C₇H₉BO₄S
badge Registry Numbers
EC Number 000-000-0
MDL Number MFCD01630820
thermostat Physical Properties
Melting Point 275-277 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of biologically active compounds and materials for organic electronics. Its boronic acid group allows for selective binding to diols, making it useful in sensor development and carbohydrate recognition studies. Additionally, it finds application in the synthesis of advanced materials for optoelectronic devices due to its ability to modify electronic properties.

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Test Parameter Specification
Purity (Titration by NaOH) 98-102%
Appearance White to tan solid
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿610.00
inventory 5g
10-20 days ฿2,660.00
inventory 25g
10-20 days ฿9,990.00
inventory 100g
10-20 days ฿35,990.00

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4-(Methanesulfonyl)phenylboronic acid
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Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of biologically active compounds and materials for organic electronics. Its boronic acid group allows for selective binding to diols, making it useful in sensor develop

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of biologically active compounds and materials for organic electronics. Its boronic acid group allows for selective binding to diols, making it useful in sensor development and carbohydrate recognition studies. Additionally, it finds application in the synthesis of advanced materials for optoelectronic devices due to its ability to modify electronic properties.

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