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 201864-71-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(3R)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]butanoic acid features a chiral (3R) backbone paired with a fluorenylmethoxycarbonyl (Fmoc) protecting group, enabling direct incorporation into peptide synthesis. This derivative delivers efficient N-terminal protection with orthogonal deprotection compatibility and enhanced solubility in organic solvents.
(3R)-3-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]butanoic acid serves as a valuable chiral building block in peptide synthesis, offering high enantiomeric purity and stability under standard coupling conditions. The Fmoc group enables efficient, orthogonal protection of primary amines, facilitating sequential chain elongation. Its robust bench stability and compatibility with common activation methods streamline purification and scale-up in medicinal chemistry workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: