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 24347-63-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-Methyl 2-hydroxy-3-methylbutanoate is a chiral ester featuring a hydroxyl group adjacent to a quaternary carbon center. This configuration imparts distinct stereochemical control in asymmetric synthesis, enabling selective functionalization in complex molecule assembly. The molecule demonstrates robust stability under standard bench conditions and integrates seamlessly into cascade reactions requiring precise spatial orientation.
(S)-Methyl 2-hydroxy-3-methylbutanoate serves as a valuable chiral building block in asymmetric synthesis, leveraging its hydroxyl and ester functionalities for downstream derivatization. The molecule exhibits bench stability and facilitates stereoselective transformations, including protection, oxidation, and coupling reactions, enabling efficient access to complex chiral intermediates. Its well-defined stereochemistry supports reproducible outcomes in medicinal chemistry and natural product synthesis workflows.
|
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: