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 790667-44-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral piperidine derivative features a bench-stable tert-butyl ester protecting group and a hydroxyl-bearing stereocenter at the 4-position, enabling selective functionalization in asymmetric synthesis. The 2-methyl substituent provides steric control, while the 1-carboxylate moiety facilitates downstream derivatization.
(2R,4R)-tert-Butyl 4-hydroxy-2-methylpiperidine-1-carboxylate serves as a stereochemically defined chiral building block for the synthesis of bioactive piperidine-containing molecules. The hydroxyl group enables facile derivatization via oxidation or substitution, while the tert-butyl carbamate provides orthogonal protection and bench stability. Its defined stereochemistry facilitates predictable transformation in medicinal chemistry campaigns and supports efficient access to complex heterocyclic scaffolds.
|
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: