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Lyciumin A

Base Information
  • Chemical Name:Lyciumin A
  • CAS No.:125708-06-7
  • Molecular Formula:C42H51 N9 O12
  • Molecular Weight:873.92
  • Hs Code.:
  • Wikidata:Q104402518
  • Mol file:125708-06-7.mol
Lyciumin A

Synonyms:Lyciumin A;125708-06-7;11-(hydroxymethyl)-2-[[3-(4-hydroxyphenyl)-2-[[1-(5-oxopyrrolidine-2-carbonyl)pyrrolidine-2-carbonyl]amino]propanoyl]amino]-3,6,9,12-tetraoxo-5-propan-2-yl-1,4,7,10,13-pentazatricyclo[14.6.1.017,22]tricosa-16(23),17,19,21-tetraene-14-carboxylic acid;LyciuminA;CHEBI:172844;AKOS040756589

Suppliers and Price of Lyciumin A
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
Total 6 raw suppliers
Chemical Property of Lyciumin A
Chemical Property:
  • XLogP3:0.3
  • Hydrogen Bond Donor Count:10
  • Hydrogen Bond Acceptor Count:12
  • Rotatable Bond Count:10
  • Exact Mass:873.36571810
  • Heavy Atom Count:63
  • Complexity:1760
Purity/Quality:

≥98% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C)C1C(=O)NCC(=O)NC(C(=O)NC(CC2=CN(C(C(=O)N1)NC(=O)C(CC3=CC=C(C=C3)O)NC(=O)C4CCCN4C(=O)C5CCC(=O)N5)C6=CC=CC=C26)C(=O)O)CO
Technology Process of Lyciumin A

There total 6 articles about Lyciumin A 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 lithium hydroxide; In N,N-dimethyl-formamide; at 20 ℃; for 2h;
DOI:10.1039/c39920001353
Guidance literature:
Multi-step reaction with 3 steps
1: 100 percent / H2 / Pd/C / dimethylformamide / 2 h
2: 64 percent / 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU) / dimethylformamide
3: 100 percent / aq. LiOH / dimethylformamide / 2 h / 20 °C
With lithium hydroxide; hydrogen; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; palladium on activated charcoal; In N,N-dimethyl-formamide;
DOI:10.1039/c39920001353
Guidance literature:
Multi-step reaction with 4 steps
1: aq. NaHCO3 / CH2Cl2
2: 100 percent / H2 / Pd/C / dimethylformamide / 2 h
3: 64 percent / 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (TBTU) / dimethylformamide
4: 100 percent / aq. LiOH / dimethylformamide / 2 h / 20 °C
With lithium hydroxide; hydrogen; sodium hydrogencarbonate; O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; palladium on activated charcoal; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1039/c39920001353
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