Introduction of CAS:133464-46-7 | FMOC-GLU(OALL)-OH
Fmoc-Glu(OAll)-OH, a synthetic amino acid, is an important component of peptides and proteins. It is a derivative of the natural amino acid glutamate, and is used in a variety of laboratory and scientific applications. Fmoc-Glu(OAll)-OH is often used in the synthesis of peptides and proteins, as it is able to form strong peptide bonds with other amino acids. It is also used in biochemical research, as it is able to interact with a wide range of biological molecules.
Specification of CAS:133464-46-7 | FMOC-GLU(OALL)-OH
|
ITEMS |
SPECIFICATION |
|
Boiling point |
650.1±55.0 °C(Predicted) |
|
Melt point |
122 - 128°C |
|
Density |
1.264±0.06 g/cm3(Predicted) |
|
Form |
Powder |
|
Color |
White |
|
Solubility |
soluble in Methanol |
|
Storage condition |
2-8°C |
Research Application of CAS:133464-46-7 | FMOC-GLU(OALL)-OH
It plays a crucial role in the self-assembly of amino acids to form unique nanostructures, which have potential applications in material chemistry and biomedical fields (Gour et al., 2021).
This compound is integral in synthesizing photocaged peptides, which are useful for studying the dynamic processes in living cells (Tang et al., 2015).
The compound is used in native chemical ligation for protein synthesis, especially in addressing challenges like poor peptide segment solubility (Giesler et al., 2021).
It is involved in the ultrasound-induced gelation of amino acids, which is significant in the development of new materials with unique properties (Geng et al., 2017).
Fmoc-Glu(OAll)-OH has applications in analytical chemistry, such as in the fluorogenic labeling for chromatographic analysis of environmental samples (Sancho et al., 1996).
It is utilized in studying the substrate recognition mechanisms of enzymes, which has implications for understanding enzymatic processes and designing enzyme inhibitors (Nakase et al., 2001).


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