4-Methyl-2-nitrobenzonitrile

>98.0%(GC)

Reagent Code: #205299
label
Alias 2-nitro-p-methylbenzidine; 4-methyl-2-nitro-benzidine;
fingerprint
CAS Number 26830-95-5

science Other reagents with same CAS 26830-95-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.15 g/mol
Formula C₈H₆N₂O₂
badge Registry Numbers
EC Number 248-019-5
MDL Number MFCD00056107
thermostat Physical Properties
Melting Point 97-99 °C(lit.)
Boiling Point 338.9°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where the nitrile and nitro groups can be further modified to form more complex molecules. Its methyl and nitro functional groups allow for selective transformations, making it valuable in fine chemical manufacturing. Also employed in research for developing new nitroaromatic compounds with potential biological activity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,630.00
10g
10-20 days ฿1,680.00
25g
10-20 days ฿4,180.00
100g
10-20 days ฿14,540.00
4-Methyl-2-nitrobenzonitrile
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where the nitrile and nitro groups can be further modified to form more complex molecules. Its methyl and nitro functional groups allow for selective transformations, making it valuable in fine chemical manufacturing. Also employed in research for developing new nitroaromatic compounds with potential biological activ

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block in organic reactions where the nitrile and nitro groups can be further modified to form more complex molecules. Its methyl and nitro functional groups allow for selective transformations, making it valuable in fine chemical manufacturing. Also employed in research for developing new nitroaromatic compounds with potential biological activity.

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