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 101327-87-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
8-Nitroquinoline-7-carbaldehyde delivers a potent electron-deficient scaffold for conjugate addition and transition-metal-catalyzed coupling reactions. The para-nitro group enhances electrophilicity at the aldehyde, enabling efficient C–C bond formation under mild conditions. This bench-stable reagent integrates readily into complex molecular architectures with high functional group tolerance.
8-Nitroquinoline-7-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling the construction of quinoline-based scaffolds through standard coupling and functional group transformation protocols. Its electron-deficient quinoline core enhances reactivity in nucleophilic additions, while the aldehyde functionality facilitates imine formation and conjugate addition reactions. Bench-stable and readily purified by column chromatography, it supports efficient synthesis of heterocyclic libraries and API intermediates.
|
GHS Pictogram :
|
GHS No : GHS08
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H341
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: