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H-Lys(Fmoc)-OH

Base Information Edit
  • Chemical Name:H-Lys(Fmoc)-OH
  • CAS No.:84624-28-2
  • Molecular Formula:C21H24N2O4
  • Molecular Weight:368.433
  • Hs Code.:2924297099
  • European Community (EC) Number:694-461-0
  • DSSTox Substance ID:DTXSID601316632
  • Nikkaji Number:J1.822.261B
  • Wikidata:Q76393671
  • Mol file:84624-28-2.mol
H-Lys(Fmoc)-OH

Synonyms:H-Lys(Fmoc)-OH;84624-28-2;N'-Fmoc-L-lysine;Nepsilon-Fmoc-L-lysine;(S)-6-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoic acid;H-L-Lys(Fmoc)-OH;N-epsilon-FMOC-L-LYSINE;(2S)-2-amino-6-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic Acid;N6-Fmoc-L-lysine;MFCD00038365;Lys(Fmoc)-OH;L-Lysine, N6-[(9H-fluoren-9-ylmethoxy)carbonyl]-;SCHEMBL10052316;DTXSID601316632;AKOS015896042;AM81975;CS-W008196;HY-W008196;DS-12986;EN300-316852;F11059;M02996;Nepsilon-(9-Fluorenylmethyloxycarbonyl)-L-lysine;N6-(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-lysine;(2S)-2-amino-6-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid;(S)-6-(((9H-fluoren-9-yl)methoxy)carbonylamino)-2-aminohexanoic acid;N-epsilon-(9-Fluorenylmethyloxycarbonyl)-L-lysine (H-L-Lys(Fmoc)-OH)

Suppliers and Price of H-Lys(Fmoc)-OH
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Nε-Fmoc-L-lysine
  • 500mg
  • $ 120.00
  • Medical Isotopes, Inc.
  • (S)-6-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-aminohexanoicacid 95+%
  • 1 g
  • $ 325.00
  • Iris Biotech GmbH
  • H-L-Lys(Fmoc)-OH
  • 1 g
  • $ 94.50
  • Iris Biotech GmbH
  • H-L-Lys(Fmoc)-OH
  • 5 g
  • $ 236.25
  • Crysdot
  • H-Lys(Fmoc)-OH 95+%
  • 100g
  • $ 376.00
  • ChemScene
  • H-Lys(Fmoc)-OH
  • 25g
  • $ 114.00
  • ChemScene
  • H-Lys(Fmoc)-OH
  • 10g
  • $ 51.00
  • ChemScene
  • H-Lys(Fmoc)-OH
  • 5g
  • $ 31.00
  • ChemScene
  • H-Lys(Fmoc)-OH
  • 100g
  • $ 385.00
  • Chem-Impex
  • Nε-Fmoc-L-lysine,99%(HPLC) 99%(HPLC)
  • 25G
  • $ 599.20
Total 68 raw suppliers
Chemical Property of H-Lys(Fmoc)-OH Edit
Chemical Property:
  • Vapor Pressure:9.96E-16mmHg at 25°C 
  • Melting Point:209-210 °C 
  • Refractive Index:1.6 
  • Boiling Point:609.9 °C at 760 mmHg 
  • PKA:2.53±0.24(Predicted) 
  • Flash Point:322.6 °C 
  • PSA:101.65000 
  • Density:1.245 g/cm3 
  • LogP:4.19850 
  • Storage Temp.:Store at RT. 
  • XLogP3:0.5
  • Hydrogen Bond Donor Count:3
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:9
  • Exact Mass:368.17360725
  • Heavy Atom Count:27
  • Complexity:490
Purity/Quality:

99% *data from raw suppliers

Nε-Fmoc-L-lysine *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCCCC(C(=O)O)N
  • Isomeric SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NCCCC[C@@H](C(=O)O)N
  • Uses Nε-Fmoc-L-lysine is an N-Fmoc-protected form of L-Lysine (L468895). L-Lysine is an essential amino acid for humans, with a suggested intake of 5-8 grams per day. L-Lysine can be found in a variety of food, such as eggs and quinoa, but is also mass produced by microbial fermentation. L-Lysine is also used as therapy to treat recurrent herpes simplex infections.
Technology Process of H-Lys(Fmoc)-OH

There total 9 articles about H-Lys(Fmoc)-OH which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With sodium sulfide; In water; at 25 - 30 ℃; for 0.166667h;
DOI:10.1016/j.tetlet.2006.05.069
Guidance literature:
With trifluoroacetic acid; In dichloromethane;
DOI:10.1002/anie.200351314
Guidance literature:
With hydrogenchloride; oxalic acid; In water; at 80 ℃; pH=1.1;
DOI:10.1139/v2012-032
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