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 1629051-80-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)heptanoic acid is a chiral, bench-stable amino acid derivative featuring a fluorenylmethyl carbamate (FMOC) protecting group. This configuration enables selective coupling in peptide synthesis, where the FMOC moiety facilitates efficient orthogonal deprotection. The aliphatic heptanoic acid chain provides solubility and compatibility with solid-phase workflows.
(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)heptanoic acid serves as a valuable chiral building block in peptide synthesis, offering high enantioselectivity and stability under standard coupling conditions. The Fmoc group enables convenient orthogonal protection of the amine, while the aliphatic carboxylic acid side chain supports diverse functionalization. Its bench-stable nature and compatibility with common purification methods make it ideal for iterative solid-phase and solution-phase peptide assembly.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: