N-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide

95%

Reagent Code: #218305
fingerprint
CAS Number 844501-78-6

science Other reagents with same CAS 844501-78-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.57 g/mol
Formula C₁₄H₁₉BClNO₃
badge Registry Numbers
MDL Number MFCD22494239
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. The acetamide moiety helps direct metalation or stabilize intermediates during synthesis. It is particularly useful in constructing biaryl structures found in bioactive compounds and functional materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿26,880.00
inventory 1g
10-20 days ฿56,000.00
N-(3-chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide
No image available

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. The acetamide moiety helps direct metalation or stabilize intermediates during synthesis. It is particularly useful in constructing biaryl structures found in bioa

Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical and agrochemical research. The acetamide moiety helps direct metalation or stabilize intermediates during synthesis. It is particularly useful in constructing biaryl structures found in bioactive compounds and functional materials.

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...