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 4425-56-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This tetrahydropyrimidine derivative features a conjugated dioxo-carbonitrile system, enabling direct integration into heterocyclic scaffolds. The electron-deficient pyrimidine core facilitates nucleophilic addition and cycloaddition reactions under mild conditions. Bench-stable and moisture-tolerant, it serves as a key intermediate in the synthesis of bioactive nitrogen-containing compounds.
2,4-Dioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile serves as a versatile building block in heterocyclic synthesis, enabling efficient access to pyrimidine-based scaffolds through nucleophilic addition and cyclization reactions. Its dual carbonyl and nitrile functionalities offer high reactivity in multicomponent condensations and support functional group tolerance under standard synthetic conditions. Bench-stable and readily purified by recrystallization, it functions as a key intermediate in the construction of biologically relevant heterocycles and is compatible with scalable reaction protocols.
|
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: