(9H-Carbazol-3-yl)boronic acid

≥95%

Reagent Code: #37144
fingerprint
CAS Number 851524-97-5

science Other reagents with same CAS 851524-97-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.02 g/mol
Formula C₁₂H₁₀BNO₂
badge Registry Numbers
MDL Number MFCD04113810
thermostat Physical Properties
Boiling Point 509.2±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

(9H-Carbazol-3-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The compound serves as a key intermediate in the preparation of carbazole derivatives, which are known for their applications in optoelectronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Additionally, it is utilized in the development of bioactive compounds and polymers with specific functional properties. Its boronic acid group facilitates efficient and selective coupling reactions, enhancing its utility in diverse chemical transformations.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Report Result
Purity (%) 95-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,190.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(9H-Carbazol-3-yl)boronic acid
No image available
(9H-Carbazol-3-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials. The compound serves as a key intermediate in the preparation of carbazole derivatives, which are known for their applications in optoelectronic materials, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Additionally, it is utilized in the development of bioactive compounds and polymers with specific functional properties. Its boronic acid group facilitates efficient and selective coupling reactions, enhancing its utility in diverse chemical transformations.
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...