(3-Phenylnaphthalen-1-yl)boronic acid
95%
Reagent
Code: #131931
CAS Number
1922905-62-1
blur_circular Chemical Specifications
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Molecular Information
Weight
248.08 g/mol
Formula
C₁₆H₁₃BO₂
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Registry Numbers
MDL Number
MFCD29472450
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Physical Properties
Boiling Point
486.0±48.0 °C(Predicted)
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Storage & Handling
Density
1.23±0.1 g/cm3(Predicted)
Storage
Room temperature, seal, inert gas
description Product Description
Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. It serves as a key building block in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables selective carbon-carbon bond formation under mild conditions, making it valuable in medicinal chemistry for constructing complex aromatic frameworks. Also applied in the preparation of fluorescent dyes and organic semiconductors due to the extended π-conjugation from the naphthalene and phenyl groups.
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