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

95%

Reagent Code: #83502
fingerprint
CAS Number 2057449-99-5

science Other reagents with same CAS 2057449-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.56956 g/mol
Formula C₁₄H₁₉BClNO₃
badge Registry Numbers
MDL Number MFCD32206450
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The boronate ester group in the molecule facilitates Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of complex organic molecules, including drug candidates and biologically active compounds. Additionally, its chloroacetamide moiety can be further functionalized, making it a versatile building block in medicinal chemistry and material science. Its application extends to the synthesis of boron-containing compounds, which are increasingly important in drug discovery and development due to their unique properties and potential therapeutic benefits.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿3,672.00
inventory 100mg
10-20 days ฿10,998.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-chloro-N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]acetamide
No image available

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The boronate ester group in the molecule facilitates Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of complex organic molecules, including drug candidates and biologically active compounds. Additionally, its chloroacetamide moiety ca

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the preparation of various pharmaceuticals and agrochemicals. The boronate ester group in the molecule facilitates Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of complex organic molecules, including drug candidates and biologically active compounds. Additionally, its chloroacetamide moiety can be further functionalized, making it a versatile building block in medicinal chemistry and material science. Its application extends to the synthesis of boron-containing compounds, which are increasingly important in drug discovery and development due to their unique properties and potential therapeutic benefits.

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...