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Product Name: | Fmoc-L-Thr-OL | CAS No: | 176380-53-3 |
---|---|---|---|
M.W: | 327.37 | MF: | C19H21NO4 |
Appearance: | White Powder | Purity: | 98+ |
EINECS No: | - | Storage: | 5-25°C |
Product Description
White Powder Fmoc-L-Thr-OL CAS NO. 176380-53-3 Purity 98+
Name: Fmoc-L-Thr-OL
CAS NO: 176380-53-3
M.W: 327.37
Appearance: White Powder
Purity: 98+
Synonyms: N-(9-FLUORENYLMETHOXYCARBONYL)-THREONINOL;N-FMOC-L-THREONINOL;9-FLUORENYLMETHYLOXYCARBONYL-L-THREONINOL;FMOC-(2R,3R)-2-AMINO-3-HYDROXY-1-BUTANOL;FMOC-THREONINOL;FMOC-THR-OL;FMOC-L-THREONINOL;FMOC-L-THR-OL
Application
Peptide Synthesis: Due to the presence of the Fmoc (9-fluorenylmethoxycarbonyl) protecting group in its structure, the compound is widely used as a building block in solid-phase peptide synthesis. It can undergo coupling reactions with other amino acids or peptide fragments to progressively build peptide chains of the desired sequence.
Organic Synthesis: Besides peptide synthesis, 2-(N-Fmoc)-Amino-1,3-butanediol also finds application as an intermediate in organic synthesis. The amino and hydroxyl functional groups in its structure allow for various chemical transformations such as esterification, amidation, reduction, and others, leading to the synthesis of other complex organic molecules.
Biochemical Research: The compound, being chiral, also finds utility in biochemical research. For instance, it can serve as a ligand for enzymes or receptors, facilitating studies on the structure-function relationships of biological macromolecules and the interactions between drugs and their targets.
Materials Science: Although not as common, in certain scenarios, the compound or its derivatives may find application as precursors for the preparation of functional materials. This depends on their specific chemical properties and interactions with other molecules.
Package
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