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Fmoc-4,5-dehydro-l-leucine

Base Information
  • Chemical Name:Fmoc-4,5-dehydro-l-leucine
  • CAS No.:87720-55-6
  • Molecular Formula:C21H21NO4
  • Molecular Weight:351.402
  • Hs Code.:29225090
  • DSSTox Substance ID:DTXSID20427199
  • Wikidata:Q82239905
  • Mol file:87720-55-6.mol
Fmoc-4,5-dehydro-l-leucine

Synonyms:fmoc-4,5-dehydro-l-leucine;87720-55-6;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpent-4-enoic acid;Fmoc-4,5-dehydro-Leu-OH;(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylpent-4-enoic acid;Fmoc-deltaLeu-OH;MFCD00237651;Fmoc-(S)-2-methallylglycine;SCHEMBL14570616;DTXSID20427199;AKOS016344241;FD21882;DS-11793;Fmoc-4,5-dehydro-L-leucine, AldrichCPR;BB 0260167;CS-0101044;EN300-7313261;A862443;(2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-methylpent-4-enoic acid;(2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-methyl-4-pentenoic acid;(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-methylpent-4-enoic?acid

Suppliers and Price of Fmoc-4,5-dehydro-l-leucine
Supply Marketing:
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-4,5-dehydro-L-leucine
  • 25mg
  • $ 312.00
  • Usbiological
  • Fmoc-4-
  • 25mg
  • $ 312.00
  • Usbiological
  • Fmoc-4-
  • 100mg
  • $ 297.00
  • Usbiological
  • Fmoc-4-
  • 100mg
  • $ 283.00
  • Usbiological
  • Fmoc-4-
  • 250mg
  • $ 273.00
  • Usbiological
  • Fmoc-4,5-dehydro-L-leucine 99+%
  • 250mg
  • $ 259.00
  • Usbiological
  • Fmoc-4-
  • 1g
  • $ 237.00
  • Usbiological
  • Fmoc-4-
  • 100mg
  • $ 233.00
  • Usbiological
  • Fmoc-4-
  • 250mg
  • $ 233.00
  • Usbiological
  • Fmoc-4-
  • 1g
  • $ 233.00
Total 24 raw suppliers
Chemical Property of Fmoc-4,5-dehydro-l-leucine
Chemical Property:
  • Boiling Point:569.8±45.0 °C(Predicted) 
  • PKA:3.74±0.10(Predicted) 
  • PSA:75.63000 
  • Density:1.223±0.06 g/cm3(Predicted) 
  • LogP:4.33540 
  • Storage Temp.:-15°C 
  • XLogP3:4.4
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:7
  • Exact Mass:351.14705815
  • Heavy Atom Count:26
  • Complexity:524
Purity/Quality:

99%, *data from raw suppliers

Fmoc-4,5-dehydro-L-leucine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=C)CC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Isomeric SMILES:CC(=C)C[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
  • Uses Fmoc-4,5-dehydro-L-leucine is a reagent in the solid-phase preparation of ε-lysylcarbonylphenoxyacetic acids to study the selective inhibition of human aldose reductase over aldehyde reductase.
Technology Process of Fmoc-4,5-dehydro-l-leucine

There total 2 articles about Fmoc-4,5-dehydro-l-leucine 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:
(R,S)-2-acetamido-4-methyl-4-pentenoic acid; With ammonium hydroxide; In water; at 33 ℃; for 24h; pH=7.2; Enzymatic reaction;
N-(9H-fluoren-2-ylmethoxycarbonyloxy)succinimide; With sodium hydrogencarbonate; In water; at 20 ℃; for 5h;
DOI:10.1002/chem.201901888
Guidance literature:
N-fluoren-9-ylmethyloxycarbonyl-4,5-dehydro-L-leucine; With 4-methyl-morpholine; pyridine; 2,6-Dichlorobenzoyl chloride; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 16h;
With piperidine; In N,N-dimethyl-formamide; at 20 ℃; for 0.5h;
N-(fluoren-9-ylmethoxycarbonyl)glycine; N-Fmoc L-Phe; Fmoc-Tyr(tBu)-OH; Further stages;
DOI:10.1002/pep2.24070
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