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 73013-68-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Acetylquinoline features a quinoline core functionalized with an acetyl group at the 6-position, delivering enhanced solubility and reactivity in synthetic transformations. This electron-deficient heterocycle integrates readily into pharmaceutical intermediates and ligand design, offering a stable, bench-ready scaffold for C–H functionalization and transition-metal-catalyzed coupling reactions.
6-Acetylquinoline serves as a versatile building block in synthetic organic chemistry, enabling efficient access to functionalized quinoline scaffolds. Its acetyl group facilitates electrophilic substitution and serves as a handle for further derivatization via aldol-type condensations or reduction to secondary alcohols. The molecule exhibits bench stability and good solubility in common organic solvents, supporting straightforward purification and integration into multi-step syntheses of heterocyclic compounds relevant to medicinal chemistry and materials science.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: