857459

N-Acetyl-L-Phenylalanin

ReagentPlus^®, 99%

• Synonym(e): (+)-N-Acetylphenylalanine, (S)-2-Acetamido-3-phenylpropanoic acid
• Lineare Formel: C₆H₅CH₂CH(NHCOCH₃)CO₂H
• CAS-Nummer: 2018-61-3
• Molekulargewicht: 207.23
• EG-Nummer: 217-959-8
• MDL-Nummer: MFCD00063158
• UNSPSC-Code: 12352209
• eCl@ss: 32160406
• PubChem Substanz-ID: 24888445
• NACRES: NA.22

Eigenschaften

• Qualitätsniveau: 100
• Produktlinie: ReagentPlus^®
• Assay: 99%
• Form: powder
• Optische Aktivität: [α]22/D +40.0°, c = 1 in methanol
• Eignung der Reaktion: reaction type: C-H Activation; reaction type: solution phase peptide synthesis; reagent type: ligand; reaction type: Peptide Synthesis
• mp (Schmelzpunkt): 171-173 °C (lit.)
• Anwendung(en): peptide synthesis
• Funktionelle Gruppe: amine; carboxylic acid
• SMILES String: CC(=O)N[C@@H](Cc1ccccc1)C(O)=O
• InChI: 1S/C11H13NO3/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9/h2-6,10H,7H2,1H3,(H,12,13)(H,14,15)/t10-/m0/s1
• InChIKey: CBQJSKKFNMDLON-JTQLQIEISA-N

Beschreibung

Allgemeine Beschreibung

N-Acetyl-L-phenylalanine is an acetyl analog of L-phenylalanine. It is widely used as a reactant to synthesize methyl or ethyl esters of N-acetyl-L-phenylalanine, which are employed as versatile building blocks in peptide synthesis.[1][2]

Anwendung

N-Acetyl-L-phenylalanine can be used as a reactant to synthesize:

• N-acetyl phenylalanine methyl ester by esterification reaction with methanol using Mukaiyama′s reagent.[2]
• Acetylaminocyclohexane propanoic acid by rhodium-catalyzed hydrogenation reaction.[3]

Rechtliche Hinweise

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable