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 1552-92-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2-cyclohexylideneacetate features a conjugated enone system flanked by a cyclohexylidene group and an ester moiety, enabling efficient participation in Michael additions and Diels-Alder reactions. This bench-stable, moisture-tolerant reagent integrates readily into synthetic sequences requiring electron-deficient alkene units.
Ethyl 2-cyclohexylideneacetate serves as a versatile Michael acceptor and enone equivalent in synthetic organic chemistry. Its conjugated enone system enables reliable nucleophilic addition, cycloaddition, and aldol-type reactions under mild conditions. The molecule exhibits good bench stability and facilitates straightforward purification, making it valuable for building complex carbocyclic and heterocyclic frameworks in medicinal chemistry and process development workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: