Benzonitrile, 4-[3-[(acetyloxy)methyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-

95%

Reagent Code: #150145
fingerprint
CAS Number 2227126-13-6

science Other reagents with same CAS 2227126-13-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.24 g/mol
Formula C₂₂H₂₄BNO₅
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in the development of new drug candidates and functional materials. The acetyloxymethyl group can act as a prodrug moiety or be hydrolyzed to release active compounds, adding utility in medicinal chemistry. Its structure supports the construction of biaryl systems found in bioactive compounds and advanced intermediates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿28,500.00
Benzonitrile, 4-[3-[(acetyloxy)methyl]-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy]-
No image available

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in the development of new drug candidates and functional materials. The acetyloxymethyl group can act as a prodrug moiety or be hydrolyzed to release active compounds, adding utility in medicinal chemistry. Its structure su

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in the development of new drug candidates and functional materials. The acetyloxymethyl group can act as a prodrug moiety or be hydrolyzed to release active compounds, adding utility in medicinal chemistry. Its structure supports the construction of biaryl systems found in bioactive compounds and advanced intermediates.

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...