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857459

Sigma-Aldrich

N-Acetyl-L-phenylalanine

ReagentPlus®, 99%

Sinonimo/i:

(+)-N-Acetylphenylalanine, (S)-2-Acetamido-3-phenylpropanoic acid

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About This Item

Formula condensata:
C6H5CH2CH(NHCOCH3)CO2H
Numero CAS:
Peso molecolare:
207.23
Numero CE:
Numero MDL:
Codice UNSPSC:
12352209
eCl@ss:
32160406
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Nome Commerciale

ReagentPlus®

Saggio

99%

Forma fisica

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

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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.

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.
  • Acetylaminocyclohexane propanoic acid by rhodium-catalyzed hydrogenation reaction.

Note legali

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

Applicazioni

N° Catalogo
Descrizione
Determinazione del prezzo

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


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