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 78610-70-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Oxoindoline-3-carbaldehyde delivers a reactive aldehyde handle and electron-deficient indoline core, enabling direct coupling in multistep synthesis. This bench-stable scaffold integrates readily into heterocyclic frameworks, serving as a key intermediate for bioactive molecule construction under standard conditions.
2-Oxoindoline-3-carbaldehyde serves as a versatile building block in medicinal chemistry, enabling efficient construction of indoline-based heterocycles. Its ortho-functionalized scaffold facilitates direct derivatization at the aldehyde and carbonyl positions, supporting diverse transformations including reductive amination, condensation reactions, and transition-metal-catalyzed couplings. The compound exhibits good bench stability and is compatible with common protecting group strategies, making it well-suited for iterative synthesis workflows in API development.
|
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: