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 912368-73-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-tert-Butyl 3-(methylamino)piperidine-1-carboxylate features a chiral piperidine core with a methylamino substituent, offering a sterically accessible nitrogen for derivatization. This bench-stable carbamate protects the amine in synthetic sequences while enabling straightforward deprotection under mild acidic conditions. The (S)-configuration ensures stereochemical fidelity in asymmetric synthesis, particularly useful in medicinal chemistry campaigns targeting CNS-active compounds.
(S)-tert-Butyl 3-(methylamino)piperidine-1-carboxylate serves as a versatile chiral building block in medicinal chemistry, enabling the efficient construction of bioactive piperidine scaffolds. Its tert-butyl carbamate group provides excellent bench stability and orthogonal deprotection compatibility, while the N-methylpiperidine moiety offers favorable solubility and metabolic stability. The compound readily participates in standard coupling reactions and functional group interconversions, facilitating rapid diversification in lead optimization campaigns.
|
GHS Pictogram :
|
GHS No : GHS06,GHS09
|
|
Signal Word : Danger
|
UN#: 2810
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H319-H410
|
|
|
Precautionary Statements : P264-P270-P273-P280-P330-P391-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: