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 14384-34-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This tetrahydrocarbazol-3-ol derivative features a stable, electron-rich carbazole core with a hydroxyl group at the 3-position, enabling direct functionalization in synthetic routes. The saturated ring system enhances solubility and handling compared to fully aromatic analogs, while the phenolic OH supports hydrogen bonding in catalytic or supramolecular applications.
2,3,4,9-Tetrahydro-1H-carbazol-3-ol serves as a versatile heterocyclic building block for medicinal chemistry and materials science. Its phenolic hydroxyl group enables direct derivatization, while the saturated carbazole core offers enhanced metabolic stability and π-conjugation potential. The compound exhibits good bench stability and facilitates efficient functionalization in standard coupling and oxidation protocols, making it valuable for scaffold diversification in API development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: