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 98276-57-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4-Diaminobenzaldehyde features two amino groups flanking a reactive aldehyde moiety, enabling selective conjugation in bioconjugation and fluorescent probe design. This electron-rich scaffold supports efficient imine formation under mild conditions and exhibits enhanced solubility in aqueous and polar organic solvents.
2,4-Diaminobenzaldehyde serves as a versatile building block in medicinal chemistry and materials science, enabling the synthesis of heterocyclic scaffolds via condensation and cyclization reactions. Its ortho-diamino functionality facilitates metal coordination and offers robust reactivity in Ugi-type multicomponent reactions. The aldehyde group supports facile derivatization through imine formation and reductive amination, while the compound exhibits good bench stability and ease of purification—key attributes for high-throughput screening and process-scale applications.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: