2-(4-(Bromomethyl)naphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
96%
Reagent
Code: #131936
CAS Number
1422655-33-1
blur_circular Chemical Specifications
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Molecular Information
Weight
347.05 g/mol
Formula
C₁₇H₂₀BBrO₂
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Registry Numbers
MDL Number
MFCD20441898
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Physical Properties
Boiling Point
439.6±28.0 °C(Predicted)
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Storage & Handling
Density
1.29±0.1 g/cm3(Predicted)
Storage
2-8°C, Sealed, Inert Gas
description Product Description
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The bromomethyl functionality allows for further derivatization, such as nucleophilic substitution or polymer functionalization, expanding its utility in materials science and drug discovery. It is particularly useful in constructing naphthalene-based conjugated systems for optoelectronic materials.
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