2-(4-Chloronaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
Reagent
Code: #130849
CAS Number
2128285-49-2
blur_circular Chemical Specifications
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Molecular Information
Weight
288.58 g/mol
Formula
C₁₆H₁₈BClO₂
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Registry Numbers
MDL Number
MFCD31735828
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Physical Properties
Boiling Point
401.6±28.0 °C(Predicted)
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Storage & Handling
Density
1.15±0.1 g/cm3(Predicted)
Storage
Room temperature, seal, dry
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in pharmaceutical and agrochemical research for constructing biaryl systems. Its boronate ester group facilitates mild and selective coupling with aryl halides, making it useful in late-stage functionalization of drug candidates. Also employed in materials science for developing organic semiconductors and conjugated polymers due to its stability and reactivity profile.
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