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 2165414-92-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral morpholine derivative features a bench-stable tert-butyl carbamate-protected amine and a methyl-substituted ring, enabling direct incorporation into peptide coupling sequences. The stereochemistry at C2 and C6 ensures high diastereoselectivity in macrocyclization reactions, while the carboxylic acid group facilitates efficient conjugation under standard coupling conditions.
(2S,6S)-4-(tert-butoxycarbonyl)-6-methylmorpholine-2-carboxylic acid serves as a versatile chiral building block for the synthesis of bioactive heterocycles and peptide mimetics. The protected amine and carboxylic acid functionalities enable orthogonal derivatization, while the stereogenic centers provide defined stereochemistry in downstream transformations. Its bench stability and compatibility with standard coupling protocols facilitate efficient access to complex scaffolds in medicinal chemistry campaigns.
|
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-P330-P362-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: