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 221313-11-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-(Trifluoromethyl)nicotinimidamide hydrochloride features a trifluoromethyl group at the 6-position of the nicotinimidamide core, enhancing electron-withdrawing character and metabolic stability. This bench-stable derivative integrates readily into heterocyclic synthesis, serving as a key building block for bioactive molecules in medicinal chemistry.
6-(Trifluoromethyl)nicotinimidamide hydrochloride serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive scaffolds via coupling reactions and cyclization protocols. The trifluoromethyl group enhances metabolic stability and membrane permeability, while the imidamide functionality offers robust reactivity in amide bond formation and transition-metal-catalyzed transformations. Bench-stable and readily purified, it facilitates scalable synthesis in medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H317
|
|
|
Precautionary Statements : P261-P264-P270-P280-P302+P352-P330-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: