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Boc-2-Methoxy-L-Phenylalanine

Boc-2-Methoxy-L-Phenylalanine Struktur
143415-63-8
CAS-Nr.
143415-63-8
Englisch Name:
Boc-2-Methoxy-L-Phenylalanine
Synonyma:
Boc-L-Phe(2-OMe)-OH;Boc-2-Methoxy-L-Phenylalanine;Boc-2-methoxy-L-phenylalanine 97%;(Tert-Butoxy)Carbonyl 2-Methoxy-L-Phenylalanine;L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2-methoxy-;(S)-2-TERT-BUTHOXYCARBONYLAMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID;(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-methoxyphenyl)propanoic acid;(2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(2-methoxyphenyl)propanoic acid;(2S)-3-(2-methoxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
CBNumber:
CB9966736
Summenformel:
C15H21NO5
Molgewicht:
295.33
MOL-Datei:
Mol file

Boc-2-Methoxy-L-Phenylalanine Eigenschaften

Schmelzpunkt:
157°C
storage temp. 
2-8°C
Aggregatzustand
powder
Farbe
White to off-white

Sicherheit

Boc-2-Methoxy-L-Phenylalanine Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Unnatural amino acid was derived from a C-H Activation methodology developed by Jin-Quan Yu and coworkers. The Pd-mediated C-C bond formation can be made in tandem with 2-Methylpyridine (Aldrich 109835).

Boc-2-Methoxy-L-Phenylalanine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Boc-2-Methoxy-L-Phenylalanine Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

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  • Boc-2-Methoxy-L-Phenylalanine
  • Boc-L-Phe(2-OMe)-OH
  • (Tert-Butoxy)Carbonyl 2-Methoxy-L-Phenylalanine
  • (2S)-2-{[(tert-butoxy)carbonyl]amino}-3-(2-methoxyphenyl)propanoic acid
  • L-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-2-methoxy-
  • Boc-2-methoxy-L-phenylalanine 97%
  • (S)-2-TERT-BUTHOXYCARBONYLAMINO-3-(2-METHOXY-PHENYL)-PROPIONIC ACID
  • (S)-2-((tert-Butoxycarbonyl)amino)-3-(2-methoxyphenyl)propanoic acid
  • (2S)-3-(2-methoxyphenyl)-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
  • 143415-63-8
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