1231709-22-0

Basic information

• Product Name: FMoc-(R)-2-aMino-2-Methylbutanoic acid
• Synonyms: FMoc-(R)-2-aMino-2-Methylbutanoic acid;FMoc-α-Me-D-Gly(Ethyl)-OH;(9H-Fluoren-9-yl)MethOxy]Carbonyl D-IsoValine
• CAS NO: 1231709-22-0
• Molecular Formula: C₂₀H₂₁NO₄
• Molecular Weight: 339.38504
• Product Categories: unnatural amino acids;α-Methyl Amino Acids
• Mol File: 1231709-22-0.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: FMoc-(R)-2-aMino-2-Methylbutanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: FMoc-(R)-2-aMino-2-Methylbutanoic acid(1231709-22-0)
• EPA Substance Registry System: FMoc-(R)-2-aMino-2-Methylbutanoic acid(1231709-22-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 22-26
• TSCA: No
• Hazardous Substances Data: 1231709-22-0(Hazardous Substances Data)

Usage

Description

FMoc-(R)-2-aMino-2-Methylbutanoic acid is a chemical compound that belongs to the family of FMoc-protected amino acids, commonly used in the field of organic chemistry. It is characterized by a (R)-2-amino-2-methylbutanoic acid unit, which is modified with an FMoc protecting group to enhance the solubility and stability of the molecule. The (R) configuration of the amino acid is significant for its stereochemistry, which is crucial for the structure and function of peptides and proteins. FMoc-(R)-2-aMino-2-Methylbutanoic acid plays a vital role in the synthesis of complex peptide structures for various biological and chemical applications.

Uses

Used in Organic Chemistry:
FMoc-(R)-2-aMino-2-Methylbutanoic acid is used as a building block for the synthesis of complex peptide structures. Its FMoc protecting group ensures the solubility and stability of the molecule during the synthesis process, facilitating the formation of desired peptide sequences.
Used in Pharmaceutical Industry:
FMoc-(R)-2-aMino-2-Methylbutanoic acid is used as a key component in the development of peptide-based drugs. Its specific stereochemistry and the ability to form complex peptide structures make it a valuable asset in designing and synthesizing therapeutic peptides with targeted biological activities.
Used in Research and Development:
FMoc-(R)-2-aMino-2-Methylbutanoic acid is utilized as a research tool in the study of peptide synthesis, protein structure, and function. Its unique properties allow scientists to explore the effects of stereochemistry on peptide conformation and biological activity, contributing to the advancement of peptide-based therapies and diagnostics.
Used in Biochemistry and Molecular Biology:
FMoc-(R)-2-aMino-2-Methylbutanoic acid serves as a versatile building block in the creation of synthetic peptides for use in biochemical and molecular biology experiments. Its ability to form complex peptide structures enables researchers to investigate the interactions between peptides and other biomolecules, such as enzymes, receptors, and nucleic acids, providing insights into fundamental biological processes and potential therapeutic targets.