2-(Trifluoromethyl)-9H-carbazole

95%

Reagent Code: #242771
fingerprint
CAS Number 2285-35-0

science Other reagents with same CAS 2285-35-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.20 g/mol
Formula C₁₃H₈F₃N
badge Registry Numbers
MDL Number MFCD09033509
thermostat Physical Properties
Melting Point 209-210 °C
Boiling Point 355.5±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.387±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used in organic electronics, particularly in the production of OLEDs (organic light-emitting diodes), as a building block for host materials in blue phosphorescent devices. Its electron-withdrawing trifluoromethyl group enhances thermal stability and electron transport properties, improving device efficiency and lifetime. Also employed in the synthesis of pharmaceuticals and agrochemicals due to its rigid aromatic structure and metabolic resistance imparted by fluorine atoms. Shows potential in photoredox catalysis and as a scaffold in materials science for developing fluorescent sensors and optoelectronic materials.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,850.00
inventory 250mg
10-20 days ฿32,770.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-(Trifluoromethyl)-9H-carbazole
No image available

Used in organic electronics, particularly in the production of OLEDs (organic light-emitting diodes), as a building block for host materials in blue phosphorescent devices. Its electron-withdrawing trifluoromethyl group enhances thermal stability and electron transport properties, improving device efficiency and lifetime. Also employed in the synthesis of pharmaceuticals and agrochemicals due to its rigid aromatic structure and metabolic resistance imparted by fluorine atoms. Shows potential in photoredo

Used in organic electronics, particularly in the production of OLEDs (organic light-emitting diodes), as a building block for host materials in blue phosphorescent devices. Its electron-withdrawing trifluoromethyl group enhances thermal stability and electron transport properties, improving device efficiency and lifetime. Also employed in the synthesis of pharmaceuticals and agrochemicals due to its rigid aromatic structure and metabolic resistance imparted by fluorine atoms. Shows potential in photoredox catalysis and as a scaffold in materials science for developing fluorescent sensors and optoelectronic materials.

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...