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Fmoc-4-nitro-L-phenylalanine

Base Information Edit
  • Chemical Name:Fmoc-4-nitro-L-phenylalanine
  • CAS No.:95753-55-2
  • Molecular Formula:C24H20N2O6
  • Molecular Weight:432.433
  • Hs Code.:2924 29 70
  • European Community (EC) Number:688-912-0
  • DSSTox Substance ID:DTXSID10426792
  • Nikkaji Number:J1.690.279I
  • Wikidata:Q72478731
  • Mol file:95753-55-2.mol
Fmoc-4-nitro-L-phenylalanine

Synonyms:95753-55-2;Fmoc-4-nitro-L-phenylalanine;Fmoc-Phe(4-NO2)-OH;Fmoc-L-4-Nitrophe;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-nitrophenyl)propanoic acid;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-nitrophenyl)propanoic acid;fmoc-p-nitro-phe-oh;N-Fmoc-4-nitro-L-phenylalanine;Fmoc-L-4-NO2-Phe-OH;Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-nitro-;MFCD00057810;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine;fmoc-4-nitrophenylalanine;N-Fmoc-4-Nitro-L-Phe-OH;SCHEMBL800312;DTXSID10426792;AKOS015837264;AC-9941;AC-9942;AM83458;CS-W011622;HY-W010906;(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-nitrophenyl)propanoic acid;PS-12015;F0443;EN300-312406;M03192;S12017;Fmoc-4-Nitro-phenylalanine Fmoc-Phe(4-NO2)-OH;Fmoc-Phe(4-NO2)-OH, >=96.0% (HPLC);A845456;J-300425;Z2044796602;(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(4-nitrophenyl)propanoic acid;N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine (Fmoc-L-Phe(4-NO2)-OH)

Suppliers and Price of Fmoc-4-nitro-L-phenylalanine
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
  • Usbiological
  • Fmoc-4-nitro-L-phenylalanine 99+%
  • 1g
  • $ 163.00
  • TRC
  • Fmoc-Phe(4-NO2)-OH
  • 25g
  • $ 745.00
  • TRC
  • Fmoc-Phe(4-NO2)-OH
  • 5g
  • $ 230.00
  • TCI Chemical
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine >98.0%(HPLC)(T)
  • 5g
  • $ 81.00
  • TCI Chemical
  • N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-4-nitro-L-phenylalanine >98.0%(HPLC)(T)
  • 1g
  • $ 27.00
  • Sigma-Aldrich
  • Fmoc-Phe(4-NO?)-OH Novabiochem?
  • 1 g
  • $ 36.80
  • Sigma-Aldrich
  • Fmoc-Phe(4-NO?)-OH Novabiochem?
  • 5 g
  • $ 141.00
  • Sigma-Aldrich
  • Fmoc-Phe(4-NO)-OHFmoc-Phe(4-NO )-OH Novabiochem . CAS 95753-55-2, molar mass 432.43 g/mol., Novabiochem
  • 8520290005
  • $ 136.00
  • Sigma-Aldrich
  • Fmoc-Phe(4-NO)-OHFmoc-Phe(4-NO )-OH Novabiochem . CAS 95753-55-2, molar mass 432.43 g/mol., Novabiochem
  • 8520290001
  • $ 35.50
  • Sigma-Aldrich
  • Fmoc-Phe(4-NO2)-OH ≥96.0% (HPLC)
  • 5g
  • $ 174.00
Total 68 raw suppliers
Chemical Property of Fmoc-4-nitro-L-phenylalanine Edit
Chemical Property:
  • Melting Point:213-223℃ 
  • Boiling Point:692.3 °C at 760 mmHg 
  • PKA:3.59±0.10(Predicted) 
  • Flash Point:372.5 °C 
  • PSA:121.45000 
  • Density:1.371 g/cm3 
  • LogP:5.04330 
  • Storage Temp.:2-8°C 
  • Solubility.:almost transparency in N,N-DMF 
  • XLogP3:4.5
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:6
  • Rotatable Bond Count:7
  • Exact Mass:432.13213636
  • Heavy Atom Count:32
  • Complexity:665
Purity/Quality:

98% *data from raw suppliers

Fmoc-4-nitro-L-phenylalanine 99+% *data from reagent suppliers

Safty Information:
  • Pictogram(s): IrritantXi 
  • Hazard Codes:Xi 
  • Safety Statements: 22-24/25 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC=C(C=C4)[N+](=O)[O-])C(=O)O
  • Isomeric SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@@H](CC4=CC=C(C=C4)[N+](=O)[O-])C(=O)O
  • Uses Fmoc-Phe(4-NO2)-OH is used to prepare squaric acid derivatives as VLA-4 integrin antagonists. It is also an intermediate used in the synthesis of analogs of kahalalide F.
Technology Process of Fmoc-4-nitro-L-phenylalanine

There total 4 articles about Fmoc-4-nitro-L-phenylalanine 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 carbonate; In 1,4-dioxane; 0 deg C, then Rt 2 h.;
DOI:10.1039/P29840001723
Guidance literature:
With trifluoroacetic acid; In water; for 1h;
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