1,2-Bis(4-nitrophenyl)ethane-1,2-dione

95%

Reagent Code: #131486
fingerprint
CAS Number 6067-45-4

science Other reagents with same CAS 6067-45-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.22 g/mol
Formula C₁₄H₈N₂O₆
badge Registry Numbers
MDL Number MFCD00093479
thermostat Physical Properties
Melting Point 213 °C
Boiling Point 532.3±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.471±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the preparation of heterocyclic compounds and dyes. Its nitro groups make it suitable for reduction reactions to form amino derivatives, which can further participate in coupling reactions for dye and pigment manufacturing. Also employed in the development of photochromic materials due to its ability to undergo reversible transformations under light exposure. Additionally, it serves as a building block in the synthesis of pharmaceuticals and agrochemicals where conjugated diketone systems are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,570.00
inventory 250mg
10-20 days ฿23,880.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,2-Bis(4-nitrophenyl)ethane-1,2-dione
No image available
Used primarily as an intermediate in organic synthesis, especially in the preparation of heterocyclic compounds and dyes. Its nitro groups make it suitable for reduction reactions to form amino derivatives, which can further participate in coupling reactions for dye and pigment manufacturing. Also employed in the development of photochromic materials due to its ability to undergo reversible transformations under light exposure. Additionally, it serves as a building block in the synthesis of pharmaceuticals
Used primarily as an intermediate in organic synthesis, especially in the preparation of heterocyclic compounds and dyes. Its nitro groups make it suitable for reduction reactions to form amino derivatives, which can further participate in coupling reactions for dye and pigment manufacturing. Also employed in the development of photochromic materials due to its ability to undergo reversible transformations under light exposure. Additionally, it serves as a building block in the synthesis of pharmaceuticals and agrochemicals where conjugated diketone systems are required.
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...