4-Nitropyridine

97%

Reagent Code: #218631
fingerprint
CAS Number 1122-61-8

science Other reagents with same CAS 1122-61-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 124.1 g/mol
Formula C₅H₄N₂O₂
badge Registry Numbers
MDL Number MFCD00054554
thermostat Physical Properties
Melting Point 500 °C (lit.)
Boiling Point 85 °C at 15 Torr (lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, 4-nitropyridine serves as a building block for nitrogen-containing heterocyclic compounds. Its nitro group allows for easy reduction to an amino group, enabling the formation of 4-aminopyridine derivatives, which are important in medicinal chemistry. It is also employed in the development of dyes and functional materials due to its electron-deficient aromatic ring, which supports various nucleophilic substitution reactions. Additionally, it finds use in coordination chemistry as a ligand precursor for metal complexes with catalytic or optical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿420.00
inventory 1g
10-20 days ฿1,650.00
inventory 5g
10-20 days ฿7,050.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Nitropyridine
No image available

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, 4-nitropyridine serves as a building block for nitrogen-containing heterocyclic compounds. Its nitro group allows for easy reduction to an amino group, enabling the formation of 4-aminopyridine derivatives, which are important in medicinal chemistry. It is also employed in the development of dyes and functional materials due to its electron-deficient aromatic ring, which supports various nucleophilic substitution reactions. Ad

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, 4-nitropyridine serves as a building block for nitrogen-containing heterocyclic compounds. Its nitro group allows for easy reduction to an amino group, enabling the formation of 4-aminopyridine derivatives, which are important in medicinal chemistry. It is also employed in the development of dyes and functional materials due to its electron-deficient aromatic ring, which supports various nucleophilic substitution reactions. Additionally, it finds use in coordination chemistry as a ligand precursor for metal complexes with catalytic or optical properties.

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...