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 368426-86-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-(Aminomethyl)-2-fluorobenzonitrile features a strategically positioned fluorine atom and nitrile group on a benzene ring, enabling selective functionalization in medicinal chemistry. The primary amine side chain facilitates conjugation or derivatization under standard conditions, offering a robust scaffold for bioactive molecule development.
5-(Aminomethyl)-2-fluorobenzonitrile serves as a versatile building block in medicinal chemistry, enabling direct incorporation of fluorinated aromatic scaffolds with orthogonal functional handles. The nitrile group facilitates downstream transformations such as amidation or reductive amination, while the primary amine supports conjugation or derivatization. Its bench-stable nature and compatibility with standard coupling protocols make it well-suited for modular synthesis of bioactive molecules, particularly in targeted kinase inhibitor and CNS drug discovery campaigns.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 3439
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301+H311+H331
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: