Bis(4-bromophenyl) Disulfide

98%(LC)

Reagent Code: #149407
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CAS Number 5335-84-2

science Other reagents with same CAS 5335-84-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.12 g/mol
Formula C₁₂H₈Br₂S₂
badge Registry Numbers
MDL Number MFCD00017832
thermostat Physical Properties
Melting Point 94 °C
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized aromatic compounds. It serves in the development of pharmaceuticals and agrochemicals due to the reactivity of the disulfide bond and the presence of bromine as a handle for cross-coupling reactions. Also employed in the synthesis of conductive polymers and organic electronic materials where controlled sulfur incorporation is required. Its stability and reactivity profile make it suitable for use in radical reactions and as a building block in materials science.

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Test Parameter Specification
Appearance solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿640.00
inventory 1g
10-20 days ฿1,330.00
inventory 5g
10-20 days ฿2,334.00

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Bis(4-bromophenyl) Disulfide
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Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized aromatic compounds. It serves in the development of pharmaceuticals and agrochemicals due to the reactivity of the disulfide bond and the presence of bromine as a handle for cross-coupling reactions. Also employed in the synthesis of conductive polymers and organic electronic materials where controlled sulfur incorporation is required. Its stability and reactivity profile make it suitable for use in radical

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized aromatic compounds. It serves in the development of pharmaceuticals and agrochemicals due to the reactivity of the disulfide bond and the presence of bromine as a handle for cross-coupling reactions. Also employed in the synthesis of conductive polymers and organic electronic materials where controlled sulfur incorporation is required. Its stability and reactivity profile make it suitable for use in radical reactions and as a building block in materials science.

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