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 1209498-46-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Amino-5-bromo-3-fluorobenzonitrile features a strategically positioned amino group and dual halogen substituents, enabling selective coupling in cross-coupling reactions. The electron-deficient aromatic core facilitates efficient Pd-catalyzed transformations, while the nitrile group provides a handle for downstream functionalization. This compound exhibits excellent bench stability under standard conditions, simplifying handling in synthetic workflows.
2-Amino-5-bromo-3-fluorobenzonitrile serves as a versatile building block in the synthesis of functionalized heterocycles and pharmaceutical intermediates. Its ortho-directed substitution pattern enables selective derivatization, while the nitrile group provides a handle for downstream transformations. The molecule exhibits good bench stability and facilitates efficient coupling reactions, making it well-suited for medicinal chemistry campaigns requiring halogenated, amino-functionalized aromatic scaffolds.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H315-H319-H332-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: