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 1393547-54-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Amino-2-chloropyrimidine-5-carbaldehyde features a reactive aldehyde group flanked by electron-rich amino and halogen-substituted pyrimidine moieties. This combination enables direct conjugation in synthetic routes targeting pharmaceutical intermediates, particularly in kinase inhibitor scaffolds. The molecule exhibits stability under standard bench conditions and facilitates efficient coupling without requiring protective group manipulation.
4-Amino-2-chloropyrimidine-5-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based heterocycles. Its amino and chloro groups offer orthogonal reactivity for downstream functionalization, while the aldehyde moiety facilitates imine formation, reductive amination, or condensation reactions. Bench-stable and compatible with standard purification methods, it functions effectively in multi-step syntheses targeting 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-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: