2-Thienyl disulfide

95%

Reagent Code: #239644
label
Alias Dithiophene disulfide;bis(2-thienyl)disulfide ether
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CAS Number 6911-51-9

science Other reagents with same CAS 6911-51-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.39 g/mol
Formula C₈H₆S₄
badge Registry Numbers
MDL Number MFCD00066333
thermostat Physical Properties
Melting Point 55-60 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a coupling agent in organic synthesis, particularly in the formation of unsymmetrical disulfides for pharmaceutical and agrochemical applications. Acts as a building block in the development of conductive polymers and organic semiconductors due to the thiophene moiety, which supports electron delocalization. Employed in surface modification of nanoparticles and electrodes to enhance electrochemical performance in sensors and energy storage devices. Also serves as a ligand in transition metal catalysis, facilitating cross-coupling reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿440.00
inventory 1g
10-20 days ฿700.00
inventory 5g
10-20 days ฿1,990.00
inventory 25g
10-20 days ฿8,450.00
inventory 100g
10-20 days ฿31,610.00
2-Thienyl disulfide
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Used as a coupling agent in organic synthesis, particularly in the formation of unsymmetrical disulfides for pharmaceutical and agrochemical applications. Acts as a building block in the development of conductive polymers and organic semiconductors due to the thiophene moiety, which supports electron delocalization. Employed in surface modification of nanoparticles and electrodes to enhance electrochemical performance in sensors and energy storage devices. Also serves as a ligand in transition metal cata

Used as a coupling agent in organic synthesis, particularly in the formation of unsymmetrical disulfides for pharmaceutical and agrochemical applications. Acts as a building block in the development of conductive polymers and organic semiconductors due to the thiophene moiety, which supports electron delocalization. Employed in surface modification of nanoparticles and electrodes to enhance electrochemical performance in sensors and energy storage devices. Also serves as a ligand in transition metal catalysis, facilitating cross-coupling reactions.

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