(3-(Phenylcarbamoyl)phenyl)boronic acid

98%

Reagent Code: #90286
fingerprint
CAS Number 397843-71-9

science Other reagents with same CAS 397843-71-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.05 g/mol
Formula C₁₃H₁₂BNO₃
badge Registry Numbers
MDL Number MFCD04115711
thermostat Physical Properties
Melting Point 250-260°C
inventory_2 Storage & Handling
Density 1.28g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceuticals and materials science. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds in drug discovery and development. Additionally, it finds application in the preparation of bioactive compounds and organic electronic materials due to its ability to introduce phenylcarbamoyl groups into target molecules. Its versatility in functional material synthesis further highlights its importance in advanced chemical research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,650.00
inventory 1g
10-20 days ฿7,860.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3-(Phenylcarbamoyl)phenyl)boronic 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 for constructing complex molecules, especially in pharmaceuticals and materials science. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds in drug discovery and development. Additionally, it finds application in the preparation of bioactive compounds and organic electronic materials due to

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in pharmaceuticals and materials science. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for creating carbon-carbon bonds in drug discovery and development. Additionally, it finds application in the preparation of bioactive compounds and organic electronic materials due to its ability to introduce phenylcarbamoyl groups into target molecules. Its versatility in functional material synthesis further highlights its importance in advanced chemical research.

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...