potassium (2,6-dimethoxyphenyl)(trifluoro)borate(1-)

98%

Reagent Code: #226155
fingerprint
CAS Number 871231-42-4

science Other reagents with same CAS 871231-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.0604 g/mol
Formula C₈H₉BF₃KO₂
thermostat Physical Properties
Melting Point >300℃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a source of the 2,6-dimethoxyphenyl group. The presence of methoxy groups enhances the stability and reactivity of the borate species, making it effective for constructing biaryl compounds under mild conditions. Its trifluoro variant improves solubility and transmetalation efficiency in catalytic cycles. Commonly applied in pharmaceutical and agrochemical research for building complex aromatic structures with high selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,800.00
inventory 5g
10-20 days ฿5,580.00
potassium (2,6-dimethoxyphenyl)(trifluoro)borate(1-)
No image available
Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a source of the 2,6-dimethoxyphenyl group. The presence of methoxy groups enhances the stability and reactivity of the borate species, making it effective for constructing biaryl compounds under mild conditions. Its trifluoro variant improves solubility and transmetalation efficiency in catalytic cycles. Commonly applied in pharmaceutical and agrochemical research for building c
Used as a reagent in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a source of the 2,6-dimethoxyphenyl group. The presence of methoxy groups enhances the stability and reactivity of the borate species, making it effective for constructing biaryl compounds under mild conditions. Its trifluoro variant improves solubility and transmetalation efficiency in catalytic cycles. Commonly applied in pharmaceutical and agrochemical research for building complex aromatic structures with high selectivity.
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...