N-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]butanamide

95%

Reagent Code: #83846
fingerprint
CAS Number 2246646-52-4

science Other reagents with same CAS 2246646-52-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.1855 g/mol
Formula C₁₆H₂₄BNO₃
badge Registry Numbers
MDL Number MFCD28098213
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in the development of pharmaceutical compounds and advanced materials. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive molecules and potential drug candidates, especially those targeting specific receptors or enzymes. Additionally, its structure allows for applications in the creation of polymers and materials with tailored properties, such as those used in electronics or coatings. Its role in medicinal chemistry research is significant, as it can serve as a building block for compounds with therapeutic potential.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,474.00
inventory 250mg
10-20 days ฿9,630.00
inventory 1g
10-20 days ฿28,620.00

Cart

No products

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

This chemical is primarily used in organic synthesis, particularly in the development of pharmaceutical compounds and advanced materials. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive molecules and potential drug candidates, especially those targeting specific receptors or enzymes. Additionally, it

This chemical is primarily used in organic synthesis, particularly in the development of pharmaceutical compounds and advanced materials. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. It is also utilized in the preparation of bioactive molecules and potential drug candidates, especially those targeting specific receptors or enzymes. Additionally, its structure allows for applications in the creation of polymers and materials with tailored properties, such as those used in electronics or coatings. Its role in medicinal chemistry research is significant, as it can serve as a building block for compounds with therapeutic potential.

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...