Potassium (2-Methoxyethyl)trifluoroborate

98%

Reagent Code: #227687
fingerprint
CAS Number 1408168-69-3

science Other reagents with same CAS 1408168-69-3

blur_circular Chemical Specifications

inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a coupling reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable and easy-to-handle source of the 2-methoxyethyl group, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates. Its trifluoroborate structure offers enhanced stability and reduced toxicity compared to traditional boronic acids, making it suitable for late-stage functionalization in complex molecule synthesis. Soluble in aqueous and organic solvents, it allows for flexible reaction conditions and efficient purification processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,400.00
inventory 250mg
10-20 days ฿11,200.00
inventory 1g
10-20 days ฿28,000.00
inventory 5g
10-20 days ฿92,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Potassium (2-Methoxyethyl)trifluoroborate
No image available

Used as a coupling reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable and easy-to-handle source of the 2-methoxyethyl group, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates. Its trifluoroborate structure offers enhanced stability and reduced toxicity compared to traditional boronic acids, making it suitable for late-stage functionalization in complex molecule synthesis. Soluble in aqueous and organic

Used as a coupling reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a stable and easy-to-handle source of the 2-methoxyethyl group, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical intermediates. Its trifluoroborate structure offers enhanced stability and reduced toxicity compared to traditional boronic acids, making it suitable for late-stage functionalization in complex molecule synthesis. Soluble in aqueous and organic solvents, it allows for flexible reaction conditions and efficient purification processes.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...