4-phenyl(naphthalene-1-yl)boronic acid
99%
Reagent
Code: #90739
CAS Number
16241-07-5
science Other reagents with same CAS 16241-07-5
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Molecular Information
Weight
248.08 g/mol
Formula
C₁₆H₁₃BO₂
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Storage & Handling
Storage
room temperature, dry
description Product Description
This chemical is widely utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a crucial building block for creating complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the development of fluorescent dyes and sensors due to its aromatic structure, which can enhance optical properties. Its stability and reactivity make it a valuable reagent in medicinal chemistry for designing drug candidates and bioactive compounds.
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