N,N,3-Trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

96%

Reagent Code: #215662
fingerprint
CAS Number 2096337-88-9

science Other reagents with same CAS 2096337-88-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.18 g/mol
Formula C₁₆H₂₄BNO₃
badge Registry Numbers
MDL Number MFCD18434458
thermostat Physical Properties
Boiling Point 439.4±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.05±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its amide functionality provides a handle for further derivatization or integration into biologically active molecules. Commonly employed in the development of pharmaceuticals and agrochemicals where aryl-aryl bond formation is required. The presence of the methyl and amide groups can influence electronic and steric properties, making it useful in fine-tuning reaction outcomes. Also applied in materials science for constructing conjugated systems in organic electronics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,650.00
inventory 1g
10-20 days ฿11,170.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N,N,3-Trimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
No image available

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its amide functionality provides a handle for further derivatization or integration into biologically active molecules. Commonly employed in the development of pharmaceuticals and agrochemicals where aryl-aryl bond formation is required. The presence of the methyl and amide groups can influence electronic and steric properties, making it useful in fine-tuning reaction outcomes. Also applied

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its amide functionality provides a handle for further derivatization or integration into biologically active molecules. Commonly employed in the development of pharmaceuticals and agrochemicals where aryl-aryl bond formation is required. The presence of the methyl and amide groups can influence electronic and steric properties, making it useful in fine-tuning reaction outcomes. Also applied in materials science for constructing conjugated systems in organic electronics.

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...