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 759-05-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Methyl-2-oxobutanoic acid features a β-keto acid scaffold with a methyl-substituted α-carbon, enhancing its reactivity in condensation and cyclization processes. This bench-stable compound integrates readily into synthetic routes requiring activated carbonyl functionality.
3-Methyl-2-oxobutanoic acid serves as a key building block in the synthesis of β-keto acids and related heterocycles. Its α-methylated ketone functionality enables facile enolization and nucleophilic addition, facilitating Michael additions and aldol-type condensations. The molecule exhibits good bench stability and is compatible with standard functional group manipulations, making it valuable for medicinal chemistry campaigns and process-scale synthesis of bioactive scaffolds.
|
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-P301+P310-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: