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 613-92-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
N'-Hydroxybenzimidamide features a hydroxylated imidamide core that enables direct participation in nitration and amidation cascades. This bench-stable reagent delivers efficient functional group interconversion under mild conditions, pairing well with electrophilic partners in synthetic sequences.
N'-Hydroxybenzimidamide serves as a reliable precursor for amidine and imidazole-based heterocycles, enabling efficient access to bioactive scaffolds through standard condensation and cyclization protocols. Its bench-stable nature and compatibility with diverse reaction conditions facilitate straightforward incorporation into medicinal chemistry workflows, particularly in the synthesis of kinase inhibitors and antiviral agents.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: