857459

N-Acetyl-L-phenylalanine

ReagentPlus^®, 99%

• Sinonimo/i: (+)-N-Acetylphenylalanine, (S)-2-Acetamido-3-phenylpropanoic acid
• Formula condensata: C₆H₅CH₂CH(NHCOCH₃)CO₂H
• Numero CAS: 2018-61-3
• Peso molecolare: 207.23
• Numero CE: 217-959-8
• Numero MDL: MFCD00063158
• Codice UNSPSC: 12352209
• eCl@ss: 32160406
• ID PubChem: 24888445
• NACRES: NA.22

Proprietà

• Livello qualitativo: 100
• Nome Commerciale: ReagentPlus^®
• Saggio: 99%
• Stato: powder
• Attività ottica: [α]22/D +40.0°, c = 1 in methanol
• Impiego in reazioni chimiche: reaction type: C-H Activation; reaction type: solution phase peptide synthesis; reagent type: ligand; reaction type: Peptide Synthesis
• Punto di fusione: 171-173 °C (lit.)
• applicazioni: peptide synthesis
• Gruppo funzionale: amine; carboxylic acid
• Stringa SMILE: 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; CBQJSKKFNMDLON-JTQLQIEISA-N

Descrizione

Descrizione generale

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]

Applicazioni

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]

Note legali

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

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable