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1333083-66-1

5-fluoro-2-(MethoxyMethyl)phenylboronic acid

Catalog#: AR009Z84  |   CAS#: 1333083-66-1  |   MDL#: MFCD14687260  |   MF: C8H10BFO3  |   MW: 183.9726

Packsize Purity Price Availability Quantity
250mg 95% $260.00 Global Stock Buy Now Add To Cart
1g 95% $745.00 Global Stock Buy Now Add To Cart
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Catalog Number AR009Z84
Chemical Name 5-fluoro-2-(MethoxyMethyl)phenylboronic acid
CAS Number 1333083-66-1
Molecular Formula C8H10BFO3
Molecular Weight 183.9726
MDL Number MFCD14687260
SMILES COCc1ccc(cc1B(O)O)F

5-Fluoro-2-(methoxymethyl)phenylboronic acid, commonly referred to as $name$, is a versatile compound widely used in chemical synthesis procedures. This compound serves as a valuable building block in the construction of various organic molecules due to its unique reactivity and ability to participate in diverse reactions.One of the key applications of 5-Fluoro-2-(methoxymethyl)phenylboronic acid in chemical synthesis is its role as a boronic acid derivative, which grants it the capability to act as a nucleophilic partner in Suzuki-Miyaura cross-coupling reactions. This reaction involves the coupling of an aryl or heteroaryl halide with an organic boronic acid in the presence of a palladium catalyst to form biaryl compounds. $name$ serves as an essential component in this transformative process, enabling the formation of complex chemical structures efficiently.Furthermore, 5-Fluoro-2-(methoxymethyl)phenylboronic acid can be utilized in the synthesis of pharmaceutical intermediates, agrochemicals, and materials with tailored properties. Its unique molecular structure and reactivity make it a valuable tool for organic chemists seeking to design and develop novel compounds with specific characteristics for various applications.In summary, $name$ plays a crucial role in chemical synthesis by serving as a versatile starting material for the construction of complex organic molecules through Suzuki-Miyaura cross-coupling reactions and other synthetic pathways. Its utility and flexibility make it an indispensable component in the toolkit of researchers and chemists working in diverse fields of chemistry.
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