• Fmoc-2-Nal-OH (CAS 112883-43-9) - TCI F1323 - AMI Scientific
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TCI

CAS 112883-43-9

Fmoc-2-Nal-OH TCI F1323

Fmoc-2-Nal-OH TCI F1323

Chemical Identity

Other names
Fmoc-3-(2-naphthyl)-L-alanine · (S)-2-[[[(9H-Fluoren-9-yl)methoxy]carbonyl]amino]-3-(naphthalen-2-yl)propanoic Acid
CAS No.
112883-43-9
Formula
C28H23NO4
Molecular weight
437.50 g/mol
Purity
>98.0%(HPLC)(T)
Storage
0-10°C
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-naphthalen-2-ylpropanoic acid
SMILES
C1=CC=C2C=C(C=CC2=C1)CC(C(=O)O)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35
InChIKey
JYUTZJVERLGMQZ-SANMLTNESA-N
MDL
MDL00144886
PubChem
CID 2734452
Rp 1.776.600,00
Rp 1.776.600,00
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TCI F1323 112883-43-9 Fmoc-2-Nal-OH is a chemical compound used in peptide synthesis, specifically in solid-phase peptide synthesis. This compound is a modified amino nitrophenyl derivative with the Fmoc (9-fluorenylmethyloxycarbonyl) protecting group. The Fmoc group is widely used in peptide chemistry to protect amino acid side chains during synthesis, allowing for controlled deprotection under specific conditions. This compound plays a critical role in the development of bioactive peptides, including antimicrobial peptides, hormones, and therapeutic agents.

The chemical properties of Fmoc-2-Nal-OH make it a preferred choice for researchers. Its stability under various reaction conditions and its ability to selectively react with specific reagents contribute to its effectiveness in peptide synthesis. The structure of the molecule allows for efficient deprotection, which simplifies the synthesis process and improves the yield of the final peptide product. These characteristics make it a reliable and essential reagent in advanced chemical biology applications.

In Indonesian laboratories, Fmoc-2-Nal-OH is commonly used in research related to chemical biology and pharmacology. It is widely utilized by research institutions and universities to develop new therapeutic compounds with potential medical applications. Its role in biotechnology and organic chemistry research further highlights its importance in the scientific community. The compound is an essential tool for researchers aiming to create bioactive peptides with precise structural and functional properties.

  • Peptide Synthesis: Fmoc-2-Nal-OH is ideal for solid-phase peptide synthesis due to its Fmoc protecting group, which allows controlled deprotection and efficient coupling reactions.
  • Bioactive Peptide Development: This compound is used to create peptides with biological activity, such as antimicrobials and hormones, by enabling precise amino acid sequence assembly.
  • Pharmaceutical Research: It supports the development of therapeutic peptides by providing a reliable building block for complex molecular structures.
  • Organic Chemistry Studies: The compound's reactivity and stability make it suitable for exploring new synthetic pathways and chemical transformations.
  • Biotechnology Applications: Fmoc-2-Nal-OH is integral to research in biotechnology, where it aids in the design of peptides for drug delivery and molecular recognition.

Brand TCI
CAS number 112883-43-9
Molecular formula —
Purity —
Category Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes Available in standard chemical reagent quantities
Physical form Solid powder
Storage Store in a cool, dry place away from light and moisture

Fmoc-2-Nal-OH should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use airtight containers, such as glass or high-density polyethylene bottles, to prevent exposure to humidity and contaminants. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment, such as gloves and safety goggles, should be worn. Avoid contact with incompatible substances, and ensure that storage conditions are consistent with standard chemical reagent safety guidelines. Proper storage ensures the compound remains effective for use in laboratory applications.

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