3-Methoxy-4-methylbenzeneboronic acid

97%

Reagent Code: #90248
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Alias 3-methoxy-4-tolueneboronic acid
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CAS Number 917757-15-4

science Other reagents with same CAS 917757-15-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.99 g/mol
Formula C₈H₁₁BO₃
badge Registry Numbers
MDL Number MFCD08274479
thermostat Physical Properties
Melting Point 192-194°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of drugs targeting neurological disorders and cancer. 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 utilized in the development of agrochemicals, contributing to the creation of herbicides and fungicides. Additionally, it finds application in material science for the preparation of advanced polymers and organic electronic materials. Its boronic acid group makes it valuable in sensor technologies for detecting sugars and other biologically relevant molecules.

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Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿1,790.00

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3-Methoxy-4-methylbenzeneboronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of drugs targeting neurological disorders and cancer. 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 utilized in the development of agrochemicals, contributing to the creation of herbicides and fungicides. Additionally, it finds application in material science for the preparation of advanced po

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of drugs targeting neurological disorders and cancer. 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 utilized in the development of agrochemicals, contributing to the creation of herbicides and fungicides. Additionally, it finds application in material science for the preparation of advanced polymers and organic electronic materials. Its boronic acid group makes it valuable in sensor technologies for detecting sugars and other biologically relevant molecules.

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