26060-97-9

Basic information

• Product Name: N-decanoylphenylalanine
• CAS NO: 26060-97-9
• Molecular Formula: C₁₉H₂₉NO₃
• Molecular Weight: 319.4385
• Mol File: 26060-97-9.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 519.4°C at 760 mmHg
• Flash Point: 267.9°C
• Density: 1.048g/cm³
• Vapor Pressure: 1.29E-11mmHg at 25°C
• Refractive Index: 1.515
• CAS DataBase Reference: N-decanoylphenylalanine(CAS DataBase Reference)
• NIST Chemistry Reference: N-decanoylphenylalanine(26060-97-9)
• EPA Substance Registry System: N-decanoylphenylalanine(26060-97-9)

Safety Data

• Hazardous Substances Data: 26060-97-9(Hazardous Substances Data)

Usage

General Description

N-Decanoylphenylalanine is a chemical compound that belongs to the class of organic compounds known as peptide and derivatives. Peptides are compounds comprised of two or more amino acid monomers linked by a peptide bond. Chemical derivatives, such as N-decanoylphenylalanine, feature functional modifications of the original peptide. In this case, N-decanoylphenylalanine is a derivative of the essential amino acid phenylalanine, with decanoyl as the functional modification. There is limited information on its specific uses and properties, but structural modifications to standard amino acids like this often have applications in biochemistry and pharmaceuticals.

Upstream product

• 334-48-5 1-decanoic acid 
• 63-91-2 L-phenylalanine 
• 75531-06-5 2-Decanoylamino-3-phenyl-propionic acid 4-nitro-phenyl ester 
• 75531-06-5 2-Decanoylamino-3-phenyl-propionic acid 4-nitro-phenyl ester 
• 112-13-0 n-decanoyl chloride 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 7524-50-7 methyl (2S)-2-amino-3-phenylpropanoate hydrochloride 
• 75536-39-9 L-N-decanoylphenylalanine p-nitrophenyl ester 

Downstream Products

• 1569832-28-5 (S)-2-(decylamino)-3-phenylpropan-1-ol 

Relevant articles and documents

New antimicrobial self-assembling short lipopeptides

Lipopeptides are an exceptional example of amphiphilic molecules that self-assemble into functional structures with applications in the areas of nanotechnology, catalysis or medicinal chemistry. Herein, we report a library of 21 short lipopeptides, together with their supramolecular characterization and antimicrobial activity against both Gram-negative (E. coli) and Gram-positive (S. aureus) strains. This study shows that simple lipoamino acids self-assemble into micellar or vesicular structures, while incorporating dipeptides capable of stablishing hydrogen bonds results in the adoption of advanced fibrilar structures. The self-assembly effect has proven to be key to achieve antimicrobial activity.

Antibacterial lipopeptides and methods for their preparation and use

Novel antibacterial lipopeptides, pharmaceutical compositions, and methods for their preparation and use are described.

Novel stereoselective incorporation and hydrolysis of long-chain amino-acid substrates by vesicular membrane systems which include tri- or tetra-peptide catalysts

In the vesicular membrane system comprising N,N-didodecyl-N,N-dimethylammonium bromide and tri- and or tetra-peptide catalysts (pH 7.68; ionic strength μ = 0.15; 298 K), Z-L-Leu-L-His-L-Leu (or Z-L-Leu-L-His-L-Leu-L-Leu), having a hydrophobic terminal L-l