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 261380-37-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-2-((tert-Butoxycarbonyl)amino)-3-(3-methoxyphenyl)propanoic acid features a chiral backbone with a bench-stable Boc-protected amine and an electron-rich para-methoxyaryl group. This configuration enables direct incorporation into peptide synthesis workflows, delivering high diastereoselectivity in coupling reactions. The aryl substituent enhances solubility in organic solvents while maintaining compatibility with standard deprotection protocols.
(R)-2-((tert-Butoxycarbonyl)amino)-3-(3-methoxyphenyl)propanoic acid serves as a valuable chiral building block for peptide synthesis and medicinal chemistry. The Boc-protected amine enables straightforward deprotection under mild acidic conditions, while the 3-methoxyphenyl group provides a well-defined aromatic handle for further functionalization. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient incorporation into complex molecular architectures.
|
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+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: