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 27372-38-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Oxo-1,4,5,6-tetrahydropyridazine-3-carboxylic acid features a conjugated β-keto carboxylic acid moiety fused to a partially saturated pyridazine ring, enabling direct incorporation into heterocyclic scaffolds. This electron-deficient core facilitates nucleophilic addition and transition-metal-catalyzed coupling reactions under mild conditions. The molecule exhibits bench-stable handling characteristics and integrates readily into medicinal chemistry campaigns targeting kinase inhibitors and bioactive heterocycles.
6-Oxo-1,4,5,6-tetrahydropyridazine-3-carboxylic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyridazine-based scaffolds. Its conjugated enone system and carboxylic acid functionality offer orthogonal reactivity for derivatization, including amidation, esterification, and nucleophilic addition. The compound exhibits bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process development in API synthesis.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: