4,4,5,5-Tetramethyl-1,3,2-dioxaborolane

97%

Reagent Code: #91226
label
Alias Pinide Borane; 4,4,5,5-Tetramethyl-1,3,2-dioxaborolane
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CAS Number 25015-63-8

science Other reagents with same CAS 25015-63-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.98 g/mol
Formula C₆H₁₃BO₂
badge Registry Numbers
MDL Number MFCD00674030
thermostat Physical Properties
Boiling Point 42-43 °C50 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.882 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Acts as a boron source in the preparation of boronic esters, which are intermediates in various chemical processes. Also employed in the development of organic electronic materials, such as OLEDs and organic semiconductors. Its stability and reactivity make it a preferred choice in complex synthetic pathways.

format_list_bulleted Product Specification

Test Parameter Specification
Purity (GC) 97-100%
Purity (Titration with NaOH) 96.5-103.5%
Refractive Index n20D 1.394-1.398
Appearance Colorless liquid
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5ml
10-20 days ฿760.00
inventory 25ml
10-20 days ฿2,180.00
inventory 100ml
10-20 days ฿6,480.00
inventory 500ml
10-20 days ฿25,380.00

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4,4,5,5-Tetramethyl-1,3,2-dioxaborolane
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Used as a reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. It is valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Acts as a boron source in the preparation of boronic esters, which are intermediates in various chemical processes. Also employed in the development of organic electronic materials, such as OLEDs and organic semiconductors. Its stability and reactivity make it a preferred choice in complex synthetic pathways.
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