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 2732-18-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5,7-Dihydroxycoumarin features a fused benzene-pyrone scaffold bearing hydroxyl groups at the 5 and 7 positions, conferring enhanced solubility and hydrogen-bonding capacity. This arrangement imparts strong electron-donating character, making it a valuable scaffold for synthesizing fluorescent probes and bioactive compounds in medicinal chemistry and natural product analogs.
5,7-Dihydroxycoumarin serves as a versatile scaffold for the synthesis of bioactive natural product analogs and pharmaceutical intermediates. Its ortho-dihydroxy substitution pattern enables facile metal coordination and oxidative coupling, while maintaining bench stability and compatibility with standard functional group manipulations. Functions effectively in esterification, glycosylation, and palladium-catalyzed cross-coupling reactions, offering reliable access to substituted coumarin derivatives used in medicinal chemistry and materials science.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H332-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: