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 1227750-73-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Fmoc-L-β-methylisoleucine integrates a sterically hindered β-methyl group into a robust Fmoc-protected amino acid scaffold. This structural modification enhances conformational rigidity and resistance to racemization during peptide synthesis, enabling efficient incorporation into challenging sequences. The Fmoc moiety supports orthogonal deprotection protocols, streamlining solid-phase workflows.
Fmoc-L-β-methylisoleucine serves as a valuable building block in peptide synthesis, offering enhanced conformational rigidity and metabolic stability. The Fmoc group enables efficient orthogonal protection, while the β-methyl substitution imparts steric hindrance that reduces racemization during coupling. This residue facilitates the incorporation of non-natural hydrophobic motifs into bioactive peptides, supporting structural diversity 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+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: