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 5623-04-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-amino-N-hydroxybenzamide features a strategically positioned hydroxylamine group conjugated to an aromatic amide, enabling direct participation in nitrosation and radical coupling reactions. The ortho-amino functionality enhances electronic delocalization, stabilizing reactive intermediates. This scaffold serves as a critical building block for bioactive heterocycles and metal-chelating ligands in medicinal chemistry applications.
2-Amino-N-hydroxybenzamide serves as a versatile building block in medicinal chemistry, enabling the synthesis of heterocyclic scaffolds through straightforward amidation and cyclization reactions. Its dual functional groups—primary amine and hydroxylamine—facilitate efficient coupling and N-oxidation transformations, offering robust utility in developing bioactive compounds with high functional group tolerance and excellent bench stability.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-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: