Bis(2-nitrophenyl) disulfide

98%

Reagent Code: #142933
label
Alias Bis(2-nitrophenyl)disulfide
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CAS Number 1155-00-6

science Other reagents with same CAS 1155-00-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.33 g/mol
Formula (O₂NC₆H₄)₂S₂
badge Registry Numbers
EC Number 214-581-5
MDL Number MFCD00007130
thermostat Physical Properties
Melting Point 194-197 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly in the formation of sulfur-containing compounds. Acts as a nitrophenyl transfer agent in cross-coupling reactions. Employed in the development of pharmaceutical intermediates where disulfide and nitro groups play a role in bioactivity. Also applied in materials science for synthesizing specialty polymers with enhanced thermal or oxidative stability due to the presence of aromatic nitro and disulfide linkages. Its photoresponsive nature makes it useful in light-sensitive chemical systems.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿290.00
inventory 100g
10-20 days ฿660.00
inventory 500g
10-20 days ฿3,150.00

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Bis(2-nitrophenyl) disulfide
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Used as a reagent in organic synthesis, particularly in the formation of sulfur-containing compounds. Acts as a nitrophenyl transfer agent in cross-coupling reactions. Employed in the development of pharmaceutical intermediates where disulfide and nitro groups play a role in bioactivity. Also applied in materials science for synthesizing specialty polymers with enhanced thermal or oxidative stability due to the presence of aromatic nitro and disulfide linkages. Its photoresponsive nature makes it useful

Used as a reagent in organic synthesis, particularly in the formation of sulfur-containing compounds. Acts as a nitrophenyl transfer agent in cross-coupling reactions. Employed in the development of pharmaceutical intermediates where disulfide and nitro groups play a role in bioactivity. Also applied in materials science for synthesizing specialty polymers with enhanced thermal or oxidative stability due to the presence of aromatic nitro and disulfide linkages. Its photoresponsive nature makes it useful in light-sensitive chemical systems.

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