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 959235-95-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-(Trifluoromethoxy)indoline features a trifluoromethoxy group at the 6-position of the indoline scaffold, conferring enhanced electron-withdrawing character and metabolic stability. This substitution pattern improves solubility in polar solvents and facilitates downstream functionalization in medicinal chemistry applications. The molecule exhibits bench-stable behavior under standard conditions and serves as a key building block for bioactive heterocycles.
6-(Trifluoromethoxy)indoline serves as a versatile building block in medicinal chemistry, enabling direct incorporation of the trifluoromethoxy group into indoline scaffolds. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient synthesis of functionalized heterocycles. The trifluoromethoxy substituent enhances metabolic stability and modulates lipophilicity, making it valuable for optimizing pharmacokinetic profiles 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: