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Fmoc-Lys-OH.HCl

Base Information Edit
  • Chemical Name:Fmoc-Lys-OH.HCl
  • CAS No.:139262-23-0
  • Molecular Formula:C21H24N2O4*ClH
  • Molecular Weight:404.894
  • Hs Code.:29242990
  • European Community (EC) Number:850-148-2
  • DSSTox Substance ID:DTXSID10474495
  • Mol file:139262-23-0.mol
Fmoc-Lys-OH.HCl

Synonyms:139262-23-0;Fmoc-Lys-OH.HCl;FMOC-LYS-OH HCL;Fmoc-Lys-OH hydrochloride;Nalpha-Fmoc-L-lysine hydrochloride;Fmoc-Lys-OH (hydrochloride);Fmoc-L-lysine hydrochloride;MFCD00190889;L-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-, hydrochloride (1:1);(2S)-6-amino-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic acid;hydrochloride;(2S)-6-amino-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acid hydrochloride;Fmoc-L-lysine HCl;Fmoc-Lys-HCL;Fmoc-Lys-OH-HCl;Fmoc-Lys-OH. HCl;Fmoc-Lys-OH inverted exclamation mark currencyHCl;Fmoc-lysine hydrochloride;N2-Fmoc-L-lysine HCl;L-Lysine, N2-[(9H-fluoren-9-ylmethoxy)carbonyl]-, monohydrochloride;(2S)-6-amino-2-(9H-fluoren-9-ylmethoxycarbonylamino)hexanoic Acid Hydrochloride;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-6-aminohexanoic acid hydrochloride;SCHEMBL20604023;DTXSID10474495;MVMZFAIUUXYFGY-FYZYNONXSA-N;AMY31301;Nalpha-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine Hydrochloride;LT0118;AKOS015908873;AKOS015924136;CS-W011691;HY-W010975;AS-12997;F0586;F10629;Fmoc-Lys-OH hydrochloride, >=98.0% (HPLC);M03421;EN300-6740520;A807512;J-007255;S-139262-23-0;(((9H-Fluoren-9-yl)methoxy)carbonyl)-L-lysine hydrochloride;(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-6-aminohexanoic acid hydrochloride;N~2~-{[(9H-Fluoren-9-yl)methoxy]carbonyl}-L-lysine--hydrogen chloride (1/1)

Suppliers and Price of Fmoc-Lys-OH.HCl
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
  • Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine Hydrochloride
  • 10mg
  • $ 45.00
  • TCI Chemical
  • Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine Hydrochloride >98.0%(HPLC)
  • 5g
  • $ 104.00
  • TCI Chemical
  • Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine Hydrochloride >98.0%(HPLC)
  • 1g
  • $ 37.00
  • SynQuest Laboratories
  • Fmoc-Lys-OH hydrochloride 98%
  • 5 g
  • $ 100.00
  • SynQuest Laboratories
  • Fmoc-Lys-OH hydrochloride 98%
  • 25 g
  • $ 295.00
  • SynQuest Laboratories
  • Fmoc-Lys-OH hydrochloride 98%
  • 100 g
  • $ 461.00
  • Sigma-Aldrich
  • Fmoc-Lys-OH hydrochloride ≥98.0% (HPLC)
  • 5g
  • $ 156.00
  • Matrix Scientific
  • Fmoc-L-lysine HCl 98%
  • 10g
  • $ 404.00
  • Matrix Scientific
  • Fmoc-L-lysine HCl 98%
  • 5g
  • $ 284.00
  • Frontier Specialty Chemicals
  • Nalpha-Fmoc-L-lysinehydrochloride 98%
  • 1g
  • $ 13.00
Total 102 raw suppliers
Chemical Property of Fmoc-Lys-OH.HCl Edit
Chemical Property:
  • Vapor Pressure:1.29E-15mmHg at 25°C 
  • Refractive Index:-11.0 ° (C=1, DMF) 
  • Boiling Point:607.6 °C at 760 mmHg 
  • Flash Point:321.3 °C 
  • PSA:101.65000 
  • LogP:5.00050 
  • Storage Temp.:2-8°C 
  • Solubility.:Soluble in dimethyl formamide (0.3g in 2ml). 
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:9
  • Exact Mass:404.1502850
  • Heavy Atom Count:28
  • Complexity:490
Purity/Quality:

≥98.0% *data from raw suppliers

Nα-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-lysine Hydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Safety Statements: 24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CCCCN)C(=O)O.Cl
  • Isomeric SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@@H](CCCCN)C(=O)O.Cl
  • Uses It is used as an active pharmaceutical intermediate and in the synthesis of nε-(7-diethylaminocoumarin-3-carboxyl)- and nε-(7-methoxycoumarin-3-carboxyl)-l-fmoc lysine as tools for protease cleavage detection by fluorescence.
Technology Process of Fmoc-Lys-OH.HCl

There total 1 articles about Fmoc-Lys-OH.HCl 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 hydrogenchloride; In diethyl ether; dichloromethane; for 16h;
DOI:10.1039/c7cc08028j
Guidance literature:
With triethylamine; In 1,4-dioxane; water; at 20 ℃; for 18h;
Guidance literature:
α-Fmoc-L-lysine hydrochloride; With N-ethyl-N,N-diisopropylamine; In water; at 20 ℃;
2-(1-hydroxyethylidene)-5,5-dimethylcyclohexane-1,3-dione; With trifluoroacetic acid; In ethanol; water; for 60h; Reflux;
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