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Fmoc-N-Me-Lys(Boc)-OH

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Fmoc-N-Me-Lys(Boc)-OH Basic information

Product Name:
Fmoc-N-Me-Lys(Boc)-OH
Synonyms:
  • N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-N-EPSILON-T-BUTYL-OXYCARBONYL-L-LYSINE
  • N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-ALPHA-METHYL-N-EPSILON-TERT-BUTYLOXYCARBONYL-L-LYSINE
  • FMOC-N-ALPHA-METHYL-N-EPSILON-T-BOC-L-LYSINE
  • FMOC-MELYS(BOC)-OH
  • FMOC-N-ME-LYS(BOC)-OH
  • FMOC-L-MELYS(BOC)-OH
  • Fmoc-Nalpha-methyl-Ne-t-Boc-L-lysine
  • N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-(tert-butoxycarbonyl)-N2-methyl-L-lysine
CAS:
197632-76-1
MF:
C27H34N2O6
MW:
482.57
Product Categories:
  • amino acids
Mol File:
197632-76-1.mol
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Fmoc-N-Me-Lys(Boc)-OH Chemical Properties

Melting point:
189-194°C (decomposition)
Boiling point:
665.4±55.0 °C(Predicted)
Density 
1.200
storage temp. 
2-8°C
pka
3.90±0.21(Predicted)
form 
Solid
color 
White to off-white
optical activity
[α]22/D -14.0°, c = 1% in chloroform
InChIKey
JMBKBGOKNZZJQA-QHCPKHFHSA-N
CAS DataBase Reference
197632-76-1
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Safety Information

WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29242990
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Fmoc-N-Me-Lys(Boc)-OH Usage And Synthesis

Description

Fmoc-N-Me-Lys(Boc)-OH is a peptide that mimics the structure of the natural substrate of serine protease. It has been shown to be stable in extracellular fluids and resistant to proteolytic degradation. The systematic sequence was designed to maximize the chance of binding to the active site of serine proteases while minimizing binding to other proteases. The maximal modifications were made on the amino acid side chains, which are most likely to interact with other proteins or with cell surfaces.

Chemical Properties

white to slight yellow to beige

Fmoc-N-Me-Lys(Boc)-OH Supplier

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