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 49744-93-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 3-(4-cyanophenyl)-3-oxopropanoate features a conjugated enone system flanked by a nitrile and ester group, enabling efficient participation in Michael additions and heterocycle formation. This electron-deficient β-ketoester integrates readily into synthetic sequences requiring controlled carbon–carbon bond construction under mild conditions.
Ethyl 3-(4-cyanophenyl)-3-oxopropanoate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted quinoline and benzothiazole scaffolds. The conjugated enone system exhibits high reactivity in nucleophilic additions and condensation reactions, while the ester and nitrile groups offer orthogonal functionalization pathways. Bench-stable and readily purified by flash chromatography, it facilitates scalable synthesis of pharmaceutically relevant intermediates.
|
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: