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 270596-49-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-fluorophenyl)butanoic acid features a chiral center at the C3 position and incorporates a fluorenylmethyl carbamate (Fmoc) protecting group, enabling its use in peptide synthesis. The para-fluorinated aryl moiety enhances lipophilicity and metabolic stability. This compound serves as a key building block for synthesizing bioactive peptides under standard coupling conditions.
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-fluorophenyl)butanoic acid serves as a chiral building block for peptide synthesis, enabling efficient incorporation of sterically demanding, fluorinated arylalanine derivatives. The Fmoc group provides orthogonal protection for primary amines, facilitating selective coupling under standard conditions. Its bench-stable solid form and compatibility with diverse coupling reagents make it ideal for both manual and automated peptide assembly workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: