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 933702-55-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloropyrimidine-5-carbaldehyde features a reactive aldehyde group flanked by a chlorine-substituted pyrimidine ring, enabling direct coupling in heterocyclic synthesis. This bench-stable electrophile integrates efficiently into medicinal chemistry scaffolds and serves as a key intermediate for bioactive compound development.
2-Chloropyrimidine-5-carbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its dual reactive functionalities—electrophilic chloro group and aldehyde moiety—enable sequential functionalization via nucleophilic substitution and carbonyl addition reactions. The compound exhibits good bench stability, facilitates straightforward purification, and supports efficient coupling with amines, thiols, and enolizable systems, making it well-suited for constructing complex pyrimidine-based scaffolds in API development workflows.
|
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: