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 98349-24-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Ethyl 2,4,5-trifluorobenzoylacetate features a trifluorinated aromatic ring that imparts enhanced electron deficiency and metabolic stability. This structural motif enables efficient coupling in C–C bond formation reactions, particularly in transition-metal-catalyzed cross-couplings. The ester functionality offers tunable reactivity and compatibility with diverse synthetic transformations.
Ethyl 2,4,5-trifluorobenzoylacetate serves as a versatile building block in synthetic organic chemistry, enabling efficient access to fluorinated heterocycles and bioactive scaffolds. Its α-acyl ketone functionality supports facile enolization and Michael addition reactions, while the trifluoromethyl-substituted aromatic ring enhances metabolic stability and lipophilicity. The ester group facilitates purification and downstream transformations, offering robust bench stability and compatibility with standard coupling and cyclization protocols.
|
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: