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 95333-14-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
7-Formylbenzofuran delivers a reactive aldehyde handle at the 7-position of a benzofuran scaffold, enabling direct conjugation in synthetic transformations. This electron-deficient heterocycle integrates readily into modular synthesis workflows, offering high stability under standard conditions and compatibility with diverse functional groups.
7-Formylbenzofuran serves as a versatile building block in synthetic organic chemistry, enabling direct functionalization at the benzofuran core through electrophilic and nucleophilic transformations. The aldehyde group facilitates reductive amination, cyanation, and transition-metal-catalyzed coupling reactions, while the fused heterocyclic framework provides structural rigidity and metabolic stability. Its bench-stable nature and compatibility with common protecting groups support efficient synthesis of complex scaffolds for medicinal chemistry and materials 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: