3-Methyl-4-nitrobenzonitrile

97%

Reagent Code: #65581
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CAS Number 96784-54-2

science Other reagents with same CAS 96784-54-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.15 g/mol
Formula C₈H₆N₂O₂
badge Registry Numbers
MDL Number MFCD00017615
thermostat Physical Properties
Melting Point 81-83°C
Boiling Point 322.2°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used primarily in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a key intermediate. It is particularly valuable in the production of herbicides and fungicides, contributing to crop protection and yield improvement. Additionally, it is utilized in organic synthesis for creating complex molecules, often in the development of dyes and pigments. Its nitro and nitrile functional groups make it a versatile building block in various chemical reactions, including nucleophilic substitutions and reductions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿288.00
1g
10-20 days ฿765.00
5g
10-20 days ฿2,961.00
3-Methyl-4-nitrobenzonitrile
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Used primarily in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a key intermediate. It is particularly valuable in the production of herbicides and fungicides, contributing to crop protection and yield improvement. Additionally, it is utilized in organic synthesis for creating complex molecules, often in the development of dyes and pigments. Its nitro and nitrile functional groups make it a versatile building block in various chemical reactions, including nucleophilic substi

Used primarily in the synthesis of pharmaceuticals and agrochemicals, this compound serves as a key intermediate. It is particularly valuable in the production of herbicides and fungicides, contributing to crop protection and yield improvement. Additionally, it is utilized in organic synthesis for creating complex molecules, often in the development of dyes and pigments. Its nitro and nitrile functional groups make it a versatile building block in various chemical reactions, including nucleophilic substitutions and reductions.

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