(3-Amino-2-methylphenyl)boronic acid hydrochloride

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Reagent Code: #113194
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CAS Number 2230901-24-1

science Other reagents with same CAS 2230901-24-1

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scatter_plot Molecular Information
Weight 187.43 g/mol
Formula C₇H₁₁BClNO₂
badge Registry Numbers
MDL Number MFCD30573866
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and diagnostic agents due to its ability to interact with diols and other biological molecules, facilitating the detection of specific analytes. Its role in medicinal chemistry is notable, as it contributes to the creation of targeted drug candidates with enhanced efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿18,108.00
inventory 250mg
10-20 days ฿3,285.00
inventory 1g
10-20 days ฿6,588.00

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(3-Amino-2-methylphenyl)boronic acid hydrochloride
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and diagnostic agents due to its ability to interact with diols and other biological molecules, f

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key intermediate for constructing complex molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of sensors and diagnostic agents due to its ability to interact with diols and other biological molecules, facilitating the detection of specific analytes. Its role in medicinal chemistry is notable, as it contributes to the creation of targeted drug candidates with enhanced efficacy and selectivity.

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