3-Nitrophenyl disulfide

98%

Reagent Code: #216648
label
Alias 3,3'-dinitrobidyldisulfide
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CAS Number 537-91-7

science Other reagents with same CAS 537-91-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.33 g/mol
Formula C₁₂H₈N₂O₄S₂
badge Registry Numbers
EC Number 208-677-6
MDL Number MFCD00007246
thermostat Physical Properties
Melting Point 78-80 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the development of sulfenylating agents, which are important in the formation of sulfur-containing compounds. Its nitro group allows for further functionalization through reduction to an amine, enabling coupling reactions in drug synthesis. Also employed in materials science for modifying surfaces and creating functional polymers with specific redox properties.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿370.00
5g
10-20 days ฿1,100.00
25g
10-20 days ฿3,320.00
100g
10-20 days ฿12,700.00
3-Nitrophenyl disulfide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the development of sulfenylating agents, which are important in the formation of sulfur-containing compounds. Its nitro group allows for further functionalization through reduction to an amine, enabling coupling reactions in drug synthesis. Also employed in materials science for modifying surfaces and creating functional polymers with specific redox properti

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block in the development of sulfenylating agents, which are important in the formation of sulfur-containing compounds. Its nitro group allows for further functionalization through reduction to an amine, enabling coupling reactions in drug synthesis. Also employed in materials science for modifying surfaces and creating functional polymers with specific redox properties.

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