Bis(neopentyl glycolato)diboron
96%
Reagent
Code: #91198
Alias
Bis(neopentylglycol) diboron 5,5,5′,5′-tetramethyl-2,2′-bis-1,3,2-dioxaborin bis(2,2-bis Methyl-1,3-propanediol) diboron
CAS Number
201733-56-4
blur_circular Chemical Specifications
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Molecular Information
Weight
225.89 g/mol
Formula
C₁₀H₂₀B₂O₄
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Registry Numbers
MDL Number
MFCD02093062
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Physical Properties
Melting Point
180.5-184.5 °C(lit.)
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Storage & Handling
Storage
2~8°C
description Product Description
Primarily utilized as a boron source in organic synthesis, this compound facilitates the borylation of aryl halides, enabling the formation of aryl boronates. These intermediates are crucial in Suzuki-Miyaura cross-coupling reactions, which are widely employed in pharmaceutical and material science industries for constructing complex organic molecules. Additionally, it serves as a reagent in the preparation of boron-containing polymers, enhancing their thermal stability and flame retardancy. Its role in catalysis and as a stabilizing agent in various chemical processes further underscores its versatility in industrial applications.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Water (Karl Fischer) | 0-0.3 |
Purity (GC) | 95.5-100 |
Appearance | White to light yellow powder or crystals |
1H NMR | Conforms to Structure |
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Bis(neopentyl glycolato)diboron
Primarily utilized as a boron source in organic synthesis, this compound facilitates the borylation of aryl halides, enabling the formation of aryl boronates. These intermediates are crucial in Suzuki-Miyaura cross-coupling reactions, which are widely employed in pharmaceutical and material science industries for constructing complex organic molecules. Additionally, it serves as a reagent in the preparation of boron-containing polymers, enhancing their thermal stability and flame retardancy. Its role in catalysis and as a stabilizing agent in various chemical processes further underscores its versatility in industrial applications.
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