Dimethyl(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Phosphine Oxide

97%

Reagent Code: #178847
fingerprint
CAS Number 1394346-20-3

science Other reagents with same CAS 1394346-20-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.11 g/mol
Formula C₁₄H₂₂BO₃P
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides under mild conditions, making it valuable in the preparation of complex organic molecules. Additionally, the phosphine oxide moiety can act as a directing group or be further modified in multi-step syntheses. Commonly applied in the development of functional materials, including organic light-emitting diodes (OLEDs) and conjugated polymers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,510.00
inventory 250mg
10-20 days ฿24,220.00
inventory 1g
10-20 days ฿72,020.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Dimethyl(4-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)Phenyl)Phosphine Oxide
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides under mild conditions, making it valuable in the preparation of complex organic molecules. Additionally, the phosphine oxide moiety can act as a directing group or be further modified in multi-step syntheses. Commonly applied in the development of functional mat

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates palladium-catalyzed coupling with aryl halides under mild conditions, making it valuable in the preparation of complex organic molecules. Additionally, the phosphine oxide moiety can act as a directing group or be further modified in multi-step syntheses. Commonly applied in the development of functional materials, including organic light-emitting diodes (OLEDs) and conjugated polymers.

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...