2,3,6,7,10,11-Hexamethoxytriphenylene

≥97%

Reagent Code: #194915
fingerprint
CAS Number 808-57-1

science Other reagents with same CAS 808-57-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 408.44 g/mol
Formula C₂₄H₂₄O₆
badge Registry Numbers
MDL Number MFCD00075571
inventory_2 Storage & Handling
Density 1.216g/mL
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of discotic liquid crystals, particularly for organic semiconductors and photovoltaic devices. Its rigid, planar structure with multiple methoxy groups enables strong π-π stacking, enhancing charge transport in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs). Also employed in the development of liquid crystalline materials for optoelectronic applications due to its ability to form columnar mesophases that support high carrier mobility. Additionally, it serves as a building block in supramolecular chemistry for creating ordered nanostructures in thin films and self-assembled materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿2,740.00
10g
10-20 days ฿5,470.00
50g
10-20 days ฿21,000.00
1g
10-20 days ฿600.00
2,3,6,7,10,11-Hexamethoxytriphenylene
No image available

Used as a key intermediate in the synthesis of discotic liquid crystals, particularly for organic semiconductors and photovoltaic devices. Its rigid, planar structure with multiple methoxy groups enables strong π-π stacking, enhancing charge transport in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs). Also employed in the development of liquid crystalline materials for optoelectronic applications due to its ability to form columnar mesophases that support high carrier

Used as a key intermediate in the synthesis of discotic liquid crystals, particularly for organic semiconductors and photovoltaic devices. Its rigid, planar structure with multiple methoxy groups enables strong π-π stacking, enhancing charge transport in organic field-effect transistors (OFETs) and organic light-emitting diodes (OLEDs). Also employed in the development of liquid crystalline materials for optoelectronic applications due to its ability to form columnar mesophases that support high carrier mobility. Additionally, it serves as a building block in supramolecular chemistry for creating ordered nanostructures in thin films and self-assembled 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...