5-Fluoro-2-nitrobenzaldehyde

98%

Reagent Code: #187196
label
Alias 5-Fluoro-2-Nitrobenzaldehyde 2-Nitrobenzaldehyde
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CAS Number 395-81-3

science Other reagents with same CAS 395-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.11 g/mol
Formula C₇H₄FNO₃
badge Registry Numbers
EC Number 206-903-8
MDL Number MFCD00153175
thermostat Physical Properties
Melting Point 92-94°C
Boiling Point 153°C 23mm
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both fluorine and nitro functional groups that enhance biological activity. Commonly employed in the preparation of dyes, fluorescent probes, and optical brighteners because of its aromatic aldehyde structure that allows for conjugation and light absorption properties. Also utilized in research for developing novel heterocyclic compounds through cyclization reactions involving the aldehyde and nitro groups. Its reactivity makes it suitable for use in multistep organic syntheses, particularly in the formation of Schiff bases and other imine derivatives used in medicinal chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,330.00
inventory 100g
10-20 days ฿5,020.00
inventory 500g
10-20 days ฿24,960.00
5-Fluoro-2-nitrobenzaldehyde
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Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both fluorine and nitro functional groups that enhance biological activity. Commonly employed in the preparation of dyes, fluorescent probes, and optical brighteners because of its aromatic aldehyde structure that allows for conjugation and light absorption properties. Also utilized in research for developing novel heterocyclic compounds through cyclization reactions involving the aldehyde and nitro groups. Its reactivity makes it suitable for use in multistep organic syntheses, particularly in the formation of Schiff bases and other imine derivatives used in medicinal chemistry.
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