5-Fluoro-2-(methoxymethyl)phenylboronic acid

98%

Reagent Code: #90884
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CAS Number 1333083-66-1

science Other reagents with same CAS 1333083-66-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.98 g/mol
Formula C₈H₁₀BFO₃
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MDL Number MFCD14687260
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create complex biaryl compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing carbon-carbon bonds. Additionally, it is utilized in the development of fluorescent probes and sensors due to its ability to interact with specific biological molecules. Its stability and reactivity make it a preferred choice in medicinal chemistry for designing drug candidates targeting various diseases.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
NMR Conforms to Structure

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inventory 1g
10-20 days ฿31,350.00

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5-Fluoro-2-(methoxymethyl)phenylboronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create complex biaryl compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing carbon-carbon bonds. Additionally, it is utilized in the development of fluorescent probes and sensors due to its ability to interact with specific biological molecules. Its st

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to create complex biaryl compounds. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing carbon-carbon bonds. Additionally, it is utilized in the development of fluorescent probes and sensors due to its ability to interact with specific biological molecules. Its stability and reactivity make it a preferred choice in medicinal chemistry for designing drug candidates targeting various diseases.

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