4-Cyclopropyl-2-(1H-imidazol-1-yl)phenylboronic acid

95%

Reagent Code: #60908
fingerprint
CAS Number 2225180-03-8

science Other reagents with same CAS 2225180-03-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.05482 g/mol
Formula C₁₂H₁₃BN₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the construction of complex molecules, often in the pharmaceutical industry for developing drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many bioactive compounds. Additionally, it may be employed in material science for designing advanced organic materials with specific electronic or structural properties. Its versatility in forming carbon-carbon bonds makes it valuable in research and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿46,782.00
inventory 5mg
10-20 days ฿16,182.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Cyclopropyl-2-(1H-imidazol-1-yl)phenylboronic acid
No image available

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the construction of complex molecules, often in the pharmaceutical industry for developing drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many bioactive compounds. Additionally, it may be employed in material science for designing advanced organic mat

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the construction of complex molecules, often in the pharmaceutical industry for developing drug candidates. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of biaryl structures, which are common in many bioactive compounds. Additionally, it may be employed in material science for designing advanced organic materials with specific electronic or structural properties. Its versatility in forming carbon-carbon bonds makes it valuable in research and industrial applications.

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...