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 134227-45-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3,4,5-Trifluorobenzonitrile delivers a trifluorinated aromatic core with a nitrile group positioned for strategic functionalization. This electron-deficient scaffold enables direct coupling reactions and serves as a key building block in pharmaceutical synthesis. The fluorine substituents enhance metabolic stability and modulate electronic properties. Its bench-stable nature simplifies handling under standard conditions.
3,4,5-Trifluorobenzonitrile serves as a versatile building block in medicinal chemistry and materials science, enabling direct functionalization at the aromatic ring due to its strong electron-withdrawing trifluoromethyl group. The nitrile functionality facilitates nucleophilic addition, amide formation, and transition-metal-catalyzed coupling reactions. Its high bench stability and compatibility with diverse reaction conditions make it ideal for constructing fluorinated heterocycles and pharmaceutical scaffolds.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 3439
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H312-H315-H319-H331-H335
|
|
|
Precautionary Statements : P261-P280-P304+P340
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: