Trimethoxyboroxine

95%

Reagent Code: #240554
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CAS Number 102-24-9

science Other reagents with same CAS 102-24-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.53 g/mol
Formula C₃H₉B₃O₆
badge Registry Numbers
MDL Number MFCD00005946
thermostat Physical Properties
Melting Point 10°C (Lit.)
Boiling Point 130°C (Lit.)
inventory_2 Storage & Handling
Density 1.1950
Storage Room temperature, seal, dry

description Product Description

Used as a boron source in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a stable and easy-to-handle reagent. It is effective in transferring boron groups to organic frameworks, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its trimethoxy structure enhances solubility in organic solvents, improving reaction efficiency. Also employed in the preparation of boronic esters and as a reagent in moisture-curing systems due to its reactivity with water, releasing methanol and forming boric acid derivatives. Useful in surface modification and adhesion promotion in coatings and composites.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿620.00
inventory 25g
10-20 days ฿2,380.00
Trimethoxyboroxine
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Used as a boron source in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a stable and easy-to-handle reagent. It is effective in transferring boron groups to organic frameworks, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its trimethoxy structure enhances solubility in organic solvents, improving reaction efficiency. Also employed in the preparation of boronic esters and as a reagent in mois

Used as a boron source in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a stable and easy-to-handle reagent. It is effective in transferring boron groups to organic frameworks, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. Its trimethoxy structure enhances solubility in organic solvents, improving reaction efficiency. Also employed in the preparation of boronic esters and as a reagent in moisture-curing systems due to its reactivity with water, releasing methanol and forming boric acid derivatives. Useful in surface modification and adhesion promotion in coatings and composites.

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