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Boc-L-homophenylalanine

Boc-L-homophenylalanine Struktur
100564-78-1
CAS-Nr.
100564-78-1
Englisch Name:
Boc-L-homophenylalanine
Synonyma:
Boc-Hphe;BOC-L-HPH;BOC-L-HPHE;BOC-HPH-OH;BOC-HFE-OH;Boc-HoMophe;Boc-Hphe-OH;Boc-HoPhe-PH;BOC-HOPHE-OH;BOC-L-HOMOPHE
CBNumber:
CB5736630
Summenformel:
C15H21NO4
Molgewicht:
279.33
MOL-Datei:
100564-78-1.mol

Boc-L-homophenylalanine Eigenschaften

Schmelzpunkt:
76-80 °C
Siedepunkt:
439.6±38.0 °C(Predicted)
Dichte
1.139
storage temp. 
2-8°C
L?slichkeit
Soluble in methanol.
pka
3.95±0.10(Predicted)
Aggregatzustand
powder to crystal
Farbe
White to Almost white
Optische Aktivit?t
[α]20/D +6.5±1°, c = 2% in ethanol
BRN 
3653506
InChIKey
MCODLPJUFHPVQP-LBPRGKRZSA-N
CAS Datenbank
100564-78-1(CAS DataBase Reference)

Sicherheit

Kennzeichnung gef?hrlicher Xi
S-S?tze: 22-24/25
WGK Germany  3
F  3-10
HazardClass  IRRITANT
HS Code  29242990

Boc-L-homophenylalanine Chemische Eigenschaften,Einsatz,Produktion Methoden

S-S?tze Betriebsanweisung:

S22:Staub nicht einatmen.
S24/25:Berührung mit den Augen und der Haut vermeiden.

Chemische Eigenschaften

White powder

Verwenden

N-Boc-L-homophenylalanine is a useful reagent for organic synthesis and other chemical processes. It is used in the preparation of piperidine-containing peptidyl proteasome inhibitors.

Boc-L-homophenylalanine Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte

Boc-L-homophenylalanine Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 375)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Chuanghai Biotechnology Co,.LTD 		+86-13131129325
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Sichuan HongRi Pharma-Tech Co.,Ltd 		+86-028-64841719 +8617390183901
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Capot Chemical Co.,Ltd. 		+86-（0）57185586718 +86-13336195806
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ATK CHEMICAL COMPANY LIMITED 		+undefined-21-51877795
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AB PharmaTech,LLC 		323-480-4688
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GenicBio Limited 		+86-21-37621270
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100564-78-1()Verwandte Suche:

  • 2-tert-Butoxycarbonylamino-4-(S)-phenylbutyric acid
  • BOC-L-HOMOPHE
  • BOC-L-HOMOPHENYL-ALA
  • Boc-Hphe-OH ,98%
  • Boc-HoPhe-PH
  • Benzenebutanoic acid, a-[[(1,1-diMethylethoxy)carbonyl]aMino]-,(
  • Boc-Hphe
  • N-ALPHA-T-BUTYLOXYCARBONYL-L-HOMO-PHENYLALANINE
  • NALPHA-tert-Butoxycarbonyl-L-homophenylalanine
  • N-alpha-t-Butyloxycarbonyl-L-homo-phenylalanine, (S)-2-(Boc-amino)-4-phenyl-butyric acid
  • (S)-2-(N-(tert-butoxycarbonyl)aMino)-4-phenylbutanoic acid
  • (S)-2-(Boc-amino)-4-phenylbutyric acid, Boc-L-homophenylalanine
  • Boc-L-Beta-homo-Phe
  • Boc-HoMophe
  • (S)-2-(tert-butoxycarbonyl)-4-phenylbutanoic acid
  • Boc-L-HomePhe-OH
  • Benzenebutanoic acid, α-[[(1,1-dimethylethoxy)carbonyl]amino]-, (αS)-
  • Boc-L-homophenylalanine99%
  • BOC-L-HOMOPHENYLALANINE
  • BOC-L-HOPHE-OH
  • BOC-L-HPH
  • BOC-L-HPHE
  • Boc-L-HPhe-OH
  • BOC-HOMO-L-PHENYLALANINE
  • BOC-HOMOPHENYLALANINE
  • BOC-HOMOPHE-OH
  • BOC-HOPHE-OH
  • BOC-HPH-OH
  • BOC-HFE-OH
  • BOC-(+)-ALPHA-AMINO-4-PHENYLBUTYRIC ACID
  • BOC-(S)-2-AMINO-4-PHENYLBUTYRIC ACID
  • L-Homophenylalanine, N-BOC protected
  • (S)-2-(tert-butoxycarbonylamino)-4-phenylbutanoic acid
  • RARECHEM BK PT 0050
  • (S)-2-(BOC-AMINO)-4-PHENYL-BUTYRIC ACID
  • (S)-2-TERT-BUTOXYCARBONYLAMINO-4-PHENYL-BUTYRIC ACID
  • T-BUTOXYCARBONYL-L-HOMOPHENYLALANINE
  • N-BOC-(L)-HOMOPHENYLALANINE
  • N-ALPHA-TERT-BUTYLOXYCARBONYL-L-HOMO-PHENYLALANINE
  • N-ALPHA-T-BOC-L-HOMOPHENYLALANINE
  • N-ALPHA-BUTOXYCARBONYL-(+)-ALPHA-AMINO-4-PHENYLBUTYRIC ACID
  • n-tert-butoxycarbonyl-l-homophenylalanine
  • (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-phenylbutanoicaci
  • Boc-L-homophenylalanine USP/EP/BP
  • L-Homophenylalanine, N-BOC protected 97%
  • N-(tert-Butoxycarbonyl)-L-homophenylalanine >
  • Boc-Hphe-OH
  • Benzenebutanoic acid, a-[[(1,1-dimethylethoxy)carbonyl]amino]-,(aS)-
  • (2S)-2-[[(2-methylpropan-2-yl)oxy-oxomethyl]amino]-4-phenylbutanoic acid
  • (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-phenylbutanoic acid
  • (Tert-Butoxy)Carbonyl HoPhe-OH
  • Carfilzomib Impurity 13
  • (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-phenylb
  • (αS)-α-[[(1,1-Dimethylethoxy)carbonyl]amino]benzenebutanoic acid
  • 100564-78-1
  • C6H5CH2CH2CHNHCOOCCH33COOH
  • Specialty Synthesis
  • Peptide Synthesis
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