857459

N-アセチル-L-フェニルアラニン

ReagentPlus^®, 99%

• 別名: (+)-N-Acetylphenylalanine, (S)-2-Acetamido-3-phenylpropanoic acid
• 化学式: C₆H₅CH₂CH(NHCOCH₃)CO₂H
• CAS番号: 2018-61-3
• 分子量: 207.23
• EC Number: 217-959-8
• MDL番号: MFCD00063158
• UNSPSCコード: 12352209
• eCl@ss: 32160406
• PubChem Substance ID: 24888445
• NACRES: NA.22

特性

• 品質水準: 100
• 製品種目: ReagentPlus^®
• アッセイ: 99%
• フォーム: powder
• 光学活性: [α]22/D +40.0°, c = 1 in methanol
• 反応適合性: reaction type: C-H Activation; reaction type: solution phase peptide synthesis; reagent type: ligand; reaction type: Peptide Synthesis
• mp: 171-173 °C (lit.)
• アプリケーション: peptide synthesis
• 官能基: amine; carboxylic acid
• SMILES記法: 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
• InChI Key: CBQJSKKFNMDLON-JTQLQIEISA-N

詳細

詳細

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]

アプリケーション

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]

法的情報

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

安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable