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 579-72-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-(N,N-Dimethylamino)benzaldehyde features a para-dimethylamino group that enhances electron density at the aromatic ring, enabling efficient conjugation with nucleophiles. This electron-rich aldehyde integrates readily into Schiff base reactions and serves as a key building block in fluorescent probe design and transition metal catalysis. The dimethylamino moiety improves solubility in organic solvents while maintaining bench stability under standard conditions.
2-(N,N-Dimethylamino)benzaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to fluorescent probes and biologically active heterocycles. Its electron-rich aromatic core and aldehyde functionality facilitate robust condensation reactions, including Mannich and Schiff base formations, with excellent bench stability and straightforward purification. This compound functions as a key intermediate in the construction of advanced pharmaceutical scaffolds and dye systems.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P261-P280-P304+P340-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: