4-Amino-3-fluorophenylboronic acid hydrochloride
97%
Reagent
Code: #90615
CAS Number
1256355-32-4
blur_circular Chemical Specifications
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Molecular Information
Weight
191.4 g/mol
Formula
C₆H₈BClFNO₂
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Registry Numbers
MDL Number
MFCD11867880
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Physical Properties
Melting Point
150-160 °C
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Storage & Handling
Storage
2-8°C, airtight, dry
description Product Description
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes, aiding in biochemical and environmental monitoring. Its fluorine substituent enhances its stability and reactivity, making it a preferred choice in various catalytic and material science applications.
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4-Amino-3-fluorophenylboronic acid hydrochloride
This compound is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a key reagent for forming carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific analytes, aiding in biochemical and environmental monitoring. Its fluorine substituent enhances its stability and reactivity, making it a preferred choice in various catalytic and material science applications.
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