Bis(neopentyl glycolato)diboron

96%

Reagent Code: #91198
label
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
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CAS Number 201733-56-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.89 g/mol
Formula C₁₀H₂₀B₂O₄
badge Registry Numbers
MDL Number MFCD02093062
thermostat Physical Properties
Melting Point 180.5-184.5 °C(lit.)
inventory_2 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.

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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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days Ft2,865.38
inventory 5g
10-20 days Ft4,298.06
inventory 25g
10-20 days Ft7,982.12
inventory 100g
10-20 days Ft30,188.79
inventory 500g
10-20 days Ft140,608.11
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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