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 606-23-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1,3-Indanedione serves as a key synthon in heterocyclic synthesis, featuring a bifunctional diketone core that enables facile cyclization and substitution. The molecule's planar structure and electron-deficient carbonyl groups facilitate nucleophilic attack, supporting efficient access to fused ring systems. This bench-stable compound integrates readily into multistep sequences for pharmaceutical intermediates and advanced materials.
1,3-Indanedione serves as a versatile building block in synthetic organic chemistry, enabling the construction of biologically relevant heterocycles through condensation reactions. Its enolizable diketone functionality facilitates efficient Michael additions and cyclocondensations, particularly in the synthesis of indole derivatives and fused polycyclic systems. The compound exhibits good bench stability and is readily purified by recrystallization, making it well-suited for routine laboratory applications in medicinal chemistry and process development.
|
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: