Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 21789-36-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4-Dimethylbenzonitrile features a nitrile group flanked by two methyl substituents at the 2- and 4-positions of the benzene ring. This electron-deficient aromatic system enhances reactivity in nucleophilic substitution processes. The methyl groups provide steric protection and improve solubility in organic solvents. This compound serves as a stable, bench-ready building block for synthesizing pharmaceutical intermediates and functional materials.
2,4-Dimethylbenzonitrile serves as a versatile building block in synthetic organic chemistry, offering enhanced stability and favorable reactivity due to the electron-donating methyl groups adjacent to the nitrile functionality. Its bench-stable nature facilitates straightforward handling and purification, while the nitrile group enables diverse transformations including hydrolysis to carboxylic acids, reduction to primary amines, or participation in nucleophilic additions. This compound functions effectively in the construction of heterocyclic scaffolds and pharmaceutical intermediates under standard reaction conditions.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H318-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P362-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: