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Usage

Uses

Used in Pharmaceutical Industry:
FMOC-(R)-3-AMINO-4-(3-METHYL-PHENYL)-BUTYRIC ACID is used as a building block in the synthesis of peptides for drug discovery and development. Its unique structure and chirality allow for the creation of complex peptide sequences that can be tailored for specific therapeutic applications.
Used in Organic Chemistry Research:
In the field of organic chemistry, FMOC-(R)-3-AMINO-4-(3-METHYL-PHENYL)-BUTYRIC ACID is used as a reagent for the synthesis of various organic compounds. Its protected functional groups facilitate controlled reactions, enabling the formation of desired products with high selectivity and yield.
Used in Peptide Synthesis:
FMOC-(R)-3-AMINO-4-(3-METHYL-PHENYL)-BUTYRIC ACID is used as a protected amino acid in solid-phase peptide synthesis. The Fmoc protecting group allows for the stepwise addition of amino acids to a growing peptide chain, with the protection being removed at each step to enable further reactions.
Used in Chiral Compounds Synthesis:
Due to its (R)-enantiomer specification, FMOC-(R)-3-AMINO-4-(3-METHYL-PHENYL)-BUTYRIC ACID is used in the synthesis of chiral compounds, which are essential in various pharmaceutical and chemical applications. The specific stereochemistry of FMOC-(R)-3-AMINO-4-(3-METHYL-PHENYL)-BUTYRIC ACID can influence the biological activity and selectivity of the resulting products.
Used in Chemical Education:
FMOC-(R)-3-AMINO-4-(3-METHYL-PHENYL)-BUTYRIC ACID is used as a teaching aid in chemical education to demonstrate the principles of stereochemistry, peptide synthesis, and the use of protecting groups in organic synthesis. It provides students with hands-on experience in handling and synthesizing complex organic molecules.

InChI:InChI=1/C26H25NO4/c1-17-7-6-8-18(13-17)14-19(15-25(28)29)27-26(30)31-16-24-22-11-4-2-9-20(22)21-10-3-5-12-23(21)24/h2-13,19,24H,14-16H2,1H3,(H,27,30)(H,28,29)/t19-/m1/s1