3-Methoxy-5-nitrobenzaldehyde

≥95%

Reagent Code: #208807
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CAS Number 354512-22-4

science Other reagents with same CAS 354512-22-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.15 g/mol
Formula C₈H₇NO₄
badge Registry Numbers
MDL Number MFCD09038015
thermostat Physical Properties
Boiling Point 326.5±27.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain anticonvulsant and anti-inflammatory drugs. It serves as a building block in organic reactions where the aldehyde group allows for further functionalization, such as in condensation reactions to form Schiff bases or heterocyclic compounds. Its nitro and methoxy substituents influence reactivity and selectivity in multi-step syntheses, making it valuable in medicinal chemistry and the development of active pharmaceutical ingredients.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,600.00
inventory 250mg
10-20 days ฿2,450.00
inventory 1g
10-20 days ฿5,980.00
inventory 5g
10-20 days ฿25,980.00
inventory 25g
10-20 days ฿80,600.00
3-Methoxy-5-nitrobenzaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain anticonvulsant and anti-inflammatory drugs. It serves as a building block in organic reactions where the aldehyde group allows for further functionalization, such as in condensation reactions to form Schiff bases or heterocyclic compounds. Its nitro and methoxy substituents influence reactivity and selectivity in multi-step syntheses, making it valuable in medicinal chemistry and the development of active
Used as an intermediate in the synthesis of pharmaceuticals, particularly in the production of certain anticonvulsant and anti-inflammatory drugs. It serves as a building block in organic reactions where the aldehyde group allows for further functionalization, such as in condensation reactions to form Schiff bases or heterocyclic compounds. Its nitro and methoxy substituents influence reactivity and selectivity in multi-step syntheses, making it valuable in medicinal chemistry and the development of active pharmaceutical ingredients.
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