2,6-Dibromo-N,N'-bis(2-ethylhexyl)-1,8:4,5-naphthalenetetracarboxdiimide

97%

Reagent Code: #173948
fingerprint
CAS Number 1088205-02-0

science Other reagents with same CAS 1088205-02-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 648.4400000000001 g/mol
Formula C₃₀H₃₆Br₂N₂O₄
badge Registry Numbers
MDL Number MFCD27923032
thermostat Physical Properties
Melting Point 245°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an n-type organic semiconductor in organic field-effect transistors (OFETs) due to its high electron mobility and stability under ambient conditions. It is particularly effective in thin-film electronics, where its planar molecular structure facilitates strong π-π stacking, enhancing charge transport. Commonly employed in flexible electronics, sensors, and printed circuits. Its solubility in common organic solvents allows for solution-processing techniques like spin-coating and inkjet printing, making it suitable for low-cost, large-area electronic devices. Also investigated in organic photovoltaics as an electron acceptor material.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,130.00
inventory 1g
10-20 days ฿4,270.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2,6-Dibromo-N,N'-bis(2-ethylhexyl)-1,8:4,5-naphthalenetetracarboxdiimide
No image available

Used as an n-type organic semiconductor in organic field-effect transistors (OFETs) due to its high electron mobility and stability under ambient conditions. It is particularly effective in thin-film electronics, where its planar molecular structure facilitates strong π-π stacking, enhancing charge transport. Commonly employed in flexible electronics, sensors, and printed circuits. Its solubility in common organic solvents allows for solution-processing techniques like spin-coating and inkjet printing, m

Used as an n-type organic semiconductor in organic field-effect transistors (OFETs) due to its high electron mobility and stability under ambient conditions. It is particularly effective in thin-film electronics, where its planar molecular structure facilitates strong π-π stacking, enhancing charge transport. Commonly employed in flexible electronics, sensors, and printed circuits. Its solubility in common organic solvents allows for solution-processing techniques like spin-coating and inkjet printing, making it suitable for low-cost, large-area electronic devices. Also investigated in organic photovoltaics as an electron acceptor material.

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...