(R)-6,7-Diphenyldibenzo[e,g][1,4]diazocine-1,12-diol

98%

Reagent Code: #229243
fingerprint
CAS Number 2648055-07-4

science Other reagents with same CAS 2648055-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 390.43 g/mol
Formula C₂₆H₁₈N₂O₂
thermostat Physical Properties
Boiling Point 538.5±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in advanced organic electronics due to its stable chiral structure and extended π-conjugation, enabling applications in chiral semiconductors and circularly polarized luminescence devices. Its rigid diazocine core supports high thermal stability, making it suitable for optoelectronic materials in OLEDs and molecular sensors. Also investigated as a scaffold in asymmetric catalysis and supramolecular chemistry for enantioselective recognition.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,500.00
inventory 250mg
10-20 days ฿11,950.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-6,7-Diphenyldibenzo[e,g][1,4]diazocine-1,12-diol
No image available

Used in advanced organic electronics due to its stable chiral structure and extended π-conjugation, enabling applications in chiral semiconductors and circularly polarized luminescence devices. Its rigid diazocine core supports high thermal stability, making it suitable for optoelectronic materials in OLEDs and molecular sensors. Also investigated as a scaffold in asymmetric catalysis and supramolecular chemistry for enantioselective recognition.

Used in advanced organic electronics due to its stable chiral structure and extended π-conjugation, enabling applications in chiral semiconductors and circularly polarized luminescence devices. Its rigid diazocine core supports high thermal stability, making it suitable for optoelectronic materials in OLEDs and molecular sensors. Also investigated as a scaffold in asymmetric catalysis and supramolecular chemistry for enantioselective recognition.

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...