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Fmoc-4-iodo-L-phenylalanine

Base Information Edit
  • Chemical Name:Fmoc-4-iodo-L-phenylalanine
  • CAS No.:82565-68-2
  • Molecular Formula:C24H20INO4
  • Molecular Weight:513.332
  • Hs Code.:2924299090
  • European Community (EC) Number:820-622-3
  • DSSTox Substance ID:DTXSID70375792
  • Nikkaji Number:J1.806.432D
  • Wikidata:Q72478506
  • Mol file:82565-68-2.mol
Fmoc-4-iodo-L-phenylalanine

Synonyms:82565-68-2;Fmoc-4-iodo-L-phenylalanine;Fmoc-Phe(4-I)-OH;Fmoc-L-4-Iodophenylalanine;Fmoc-4'-iodo-L-Phe;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-iodophenyl)propanoic acid;Fmoc-L-Phe(4-I);L-Phenylalanine, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-4-iodo-;MFCD00672340;Fmoc-L-Phe(4-I)-OH;Fmoc-p-iodo-Phe-OH;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(4-iodophenyl)propanoic acid;N-Fmoc-4-iodo-L-phenylalanine;SCHEMBL118297;N-FMOC-p-Iodo-L-phenylalanine;DTXSID70375792;AKOS007930320;AKOS015912059;AC-9915;AM83379;CS-W014430;HY-W013714;Fmoc-Phe(4-I)-OH, >=97.0%;DS-15347;A50201;EN300-3422139;A840373;Fmoc-L-4-iodophenylalanine (Fmoc-L-Phe(4-I)-OH);J-300414;N-(9H-Fluorene-9-ylmethoxycarbonyl)-4-iodo-L-phenylalanine;(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(4-iodophenyl)propanoic acid;(S)-2-(((9H-fluoren-9-yl)methoxy)carbonylamino)-3-(4-iodophenyl)propanoic acid

Suppliers and Price of Fmoc-4-iodo-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-iodo-L-phenylalanine
  • 2g
  • $ 333.00
  • TRC
  • Fmoc-4-iodo-L-phenylalanine
  • 500mg
  • $ 65.00
  • TRC
  • Fmoc-4-iodo-L-phenylalanine
  • 100mg
  • $ 45.00
  • SynQuest Laboratories
  • 4-Iodo-L-phenylalanine, N-Fmoc protected 98%
  • 1 g
  • $ 26.00
  • SynQuest Laboratories
  • 4-Iodo-L-phenylalanine, N-Fmoc protected 98%
  • 5 g
  • $ 80.00
  • SynQuest Laboratories
  • 4-Iodo-L-phenylalanine, N-Fmoc protected 98%
  • 25 g
  • $ 303.00
  • Sigma-Aldrich
  • Fmoc-Phe(4-I)-OH ≥97.0%
  • 5g-f
  • $ 711.00
  • Sigma-Aldrich
  • Fmoc-Phe(4-I)-OH ≥97.0%
  • 5 g
  • $ 302.00
  • Sigma-Aldrich
  • Fmoc-Phe(4-I)-OH ≥97.0%
  • 1g-f
  • $ 138.00
  • Sigma-Aldrich
  • Fmoc-Phe(4-I)-OH ≥97.0%
  • 1 g
  • $ 89.00
Total 68 raw suppliers
Chemical Property of Fmoc-4-iodo-L-phenylalanine Edit
Chemical Property:
  • Appearance/Colour:White powder 
  • Vapor Pressure:2.97E-18mmHg at 25°C 
  • Melting Point:213-217 °C(lit.) 
  • Refractive Index:1.668 
  • Boiling Point:658.8oC at 760 mmHg 
  • PKA:3.73±0.10(Predicted) 
  • Flash Point:352.2oC 
  • PSA:75.63000 
  • Density:1.577g/cm3 
  • LogP:5.21650 
  • Storage Temp.:2-8°C 
  • Sensitive.:Light Sensitive 
  • XLogP3:5.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:7
  • Exact Mass:513.04371
  • Heavy Atom Count:30
  • Complexity:584
Purity/Quality:

96% 1H NMR *data from raw suppliers

Fmoc-4-iodo-L-phenylalanine *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)I)C(=O)O
  • Isomeric SMILES:C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@@H](CC4=CC=C(C=C4)I)C(=O)O
  • Uses Synthesis of a phosphotyrosine mimetic
Technology Process of Fmoc-4-iodo-L-phenylalanine

There total 3 articles about Fmoc-4-iodo-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 N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 0 - 25 ℃;
DOI:10.1002/chem.201200952
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