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 321524-83-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylbutanoic acid serves as a chiral building block for peptide synthesis, featuring a fluorenylmethyl carbamate (Fmoc) protecting group and a sterically defined side chain. This configuration enables efficient coupling under standard conditions, with the phenylbutanoyl moiety providing structural rigidity and enhanced solubility in organic media.
(2S,3R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-phenylbutanoic acid serves as a well-established chiral building block for peptide synthesis, offering high stereochemical fidelity and compatibility with standard coupling protocols. The Fmoc group enables convenient N-terminal protection with orthogonal deprotection under mild basic conditions. Its phenyl-substituted aliphatic side chain provides structural rigidity and enhances metabolic stability, making it suitable for the synthesis of bioactive peptides and peptidomimetics requiring defined stereochemistry and improved solubility.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: