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Merck

857459

Sigma-Aldrich

N-Acetyl-L-Phenylalanin

ReagentPlus®, 99%

Synonym(e):

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

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About This Item

Lineare Formel:
C6H5CH2CH(NHCOCH3)CO2H
CAS-Nummer:
Molekulargewicht:
207.23
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352209
eCl@ss:
32160406
PubChem Substanz-ID:
NACRES:
NA.22

Qualitätsniveau

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

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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.

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

Rechtliche Hinweise

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

Anwendung

Produkt-Nr.
Beschreibung
Preisangaben

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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