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 313279-12-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Amino-3-nitrobenzamide features a strategically positioned amino group ortho to a nitro functionality, enabling direct participation in coupling reactions. This electron-deficient aromatic scaffold integrates readily into complex heterocycles and serves as a key building block in medicinal chemistry. The amide linkage enhances solubility and facilitates derivatization under mild conditions.
2-Amino-3-nitrobenzamide serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds via cyclization reactions. Its ortho-dinitro substitution pattern facilitates controlled functionalization, while the amino and amide groups offer complementary handles for derivatization. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for iterative synthesis workflows in API development.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3259
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: