(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid

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Reagent Code: #90882
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CAS Number 1333392-80-5

science Other reagents with same CAS 1333392-80-5

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Weight 212.02 g/mol
Formula C₁₀H₁₄BFO₃
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MDL Number MFCD14687289
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and drug candidates. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the construction of diverse aromatic structures. Additionally, it may be utilized in the development of sensors and diagnostic agents due to its ability to interact with specific biological targets.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿35,150.00

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(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid
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(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and drug candidates. Its boronic acid group facilitates efficient coupling with aryl ha

(5-fluoro-2-(isopropoxymethyl)phenyl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound acts as a key intermediate in the synthesis of complex organic molecules, including bioactive compounds and drug candidates. Its boronic acid group facilitates efficient coupling with aryl halides, enabling the construction of diverse aromatic structures. Additionally, it may be utilized in the development of sensors and diagnostic agents due to its ability to interact with specific biological targets.

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