(S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]butanoic Acid TCI F1247

Chemical Identity

Other names: Fmoc-Abu-OH · Fmoc-L-alpha-Aminobutyric Acid
CAS No.: 135112-27-5
Formula: C19H19NO4
Molecular weight: 325.36 g/mol
Purity: >98.0%(HPLC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid
SMILES: CCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
InChIKey: XQIRYUNKLVPVRR-KRWDZBQOSA-N
MDL: MDL00080268
PubChem: CID 853016

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(S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]butanoic Acid is a specialized chemical compound used in advanced laboratory research, particularly in organic and biochemical applications. This compound plays a critical role in the synthesis of complex molecules, especially in peptide chemistry and the development of biologically active substances. Its unique molecular structure enables it to participate in a wide range of chemical reactions, making it a valuable tool for researchers aiming to create compounds with specific functional properties.

The compound's molecular structure features a fluoren-9-yl methoxy carbonyl group, which contributes to its stability and reactivity in chemical environments. This combination of properties allows it to be an essential reagent in the synthesis of bioactive molecules. Its high reactivity and structural complexity make it a preferred choice for applications requiring precise chemical control and high specificity. Additionally, its solubility in organic solvents simplifies handling and purification processes in laboratory settings.

In Indonesian laboratories, this compound is commonly used in research focused on drug development, medical diagnostics, and biomedical studies. Its role in synthesizing compounds with therapeutic potential makes it a key component in the work of chemists and biochemists. The compound's versatility and reliability make it a staple in laboratories that require high-quality reagents for complex chemical processes.

Peptide Synthesis: This compound is ideal for constructing peptide sequences due to its reactive functional groups, enabling efficient coupling reactions in solid-phase peptide synthesis.
Bioactive Compound Development: Its structural features make it suitable for synthesizing molecules with biological activity, supporting research in pharmaceutical and biotechnology fields.
Organic Chemistry Research: The compound's reactivity and stability make it a valuable reagent in the synthesis of complex organic molecules.
Medical Diagnostics: It is used in the development of diagnostic reagents that require precise chemical interactions and stable molecular structures.
Biomedical Research: Its role in creating biologically active compounds supports studies in drug discovery and therapeutic applications.

Brand	TCI
CAS number	135112-27-5
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in various quantities as per standard supplier offerings
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation when working with this compound to minimize exposure. Storage conditions should be consistent to avoid any changes in its physical or chemical properties, ensuring its effectiveness in research applications.

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