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 5305-40-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4,6-Dichloropyrimidine-5-carbaldehyde delivers a reactive aldehyde handle flanked by two electron-withdrawing chlorine atoms, enabling efficient coupling in nucleophilic addition reactions. This bench-stable heterocycle integrates readily into pharmaceutical intermediates and functional materials, offering high chemoselectivity under standard conditions.
4,6-Dichloropyrimidine-5-carbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its electrophilic aldehyde group enables efficient functionalization via nucleophilic addition, while the dichloropyrimidine core supports transition-metal-catalyzed coupling reactions. The compound exhibits good bench stability and facilitates the construction of complex pyrimidine-based scaffolds common in kinase inhibitors and antiviral agents.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H317-H319
|
|
|
Precautionary Statements : P261-P264-P270-P272-P280-P302+P352-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: