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 1257848-48-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-2-(4-(Tert-butoxycarbonyl)morpholin-2-yl)acetic acid features a chiral morpholine-bearing side chain with a protected amine, enabling direct incorporation into peptide synthesis. The tert-butyl carbamate group ensures stability during conjugation workflows and facilitates selective deprotection under mild acidic conditions. This derivative delivers precise stereochemical control in bioactive molecule construction.
(R)-2-(4-(Tert-Butoxycarbonyl)morpholin-2-yl)acetic acid serves as a versatile chiral building block for the synthesis of bioactive molecules, enabling efficient access to morpholine-containing scaffolds. The tert-butyl ester group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. Its well-defined stereochemistry and functional group tolerance make it ideal for peptide coupling and late-stage diversification in medicinal chemistry 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: