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 25384-14-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-(2-Aminophenyl)ethanone hydrochloride features a benzene ring bearing both an amino group and a ketone functionality, enabling direct coupling in transition metal-catalyzed reactions. The protonated amine enhances solubility in aqueous media while maintaining stability under standard bench conditions. This form facilitates efficient incorporation into pharmaceutical intermediates and functionalized aromatic scaffolds.
1-(2-Aminophenyl)ethanone hydrochloride serves as a versatile building block for the synthesis of heterocyclic scaffolds and bioactive molecules. Its ortho-aminobenzoyl functionality enables direct participation in cyclization reactions, including imine formation and electrophilic substitution. The hydrochloride salt enhances solubility and stability in aqueous and polar organic media, facilitating handling and purification in standard synthetic workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: