Vincamine N-oxide

Base Information

• Chemical Name: Vincamine N-oxide
• CAS No.: 51442-60-5
• Molecular Formula: C21H26N2O4
• Molecular Weight: 370.4421
• DSSTox Substance ID: DTXSID70965758
• Wikidata: Q82948061
• Metabolomics Workbench ID: 122441
• ChEMBL ID: CHEMBL1164480

Synonyms:Vincamine N-oxide;Alpneumine G;N-Oxyde de Vincamine [French];N-Oxyde de Vincamine;51442-60-5;CHEMBL1164480;Eburnamenine-14-carboxylic acid, 14,15-dihydro-14-hydroxy-, methyl ester, 4-oxide, (3-alpha,14-beta,16-alpha)-;DTXSID70965758;BDBM50321285;LS-63693;Methyl 13a-ethyl-12-hydroxy-4-oxo-1,2,3,4,5,6,12,13,13a,13b-decahydro-4lambda~5~-indolo[3,2,1-de]pyrido[3,2,1-ij][1,5]naphthyridine-12-carboxylate

Chemical Property of Vincamine N-oxide

Chemical Property:

• Melting Point: 280 °C
• Boiling Point: °Cat760mmHg
• PKA: 11.59±0.40(Predicted)
• Flash Point: °C
• PSA: 80.89000
• Density: g/cm³
• LogP: 2.92390
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 3
• Exact Mass: 370.18925731
• Heavy Atom Count: 27
• Complexity: 644

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCC12CCC[N+]3(C1C4=C(CC3)C5=CC=CC=C5N4C(C2)(C(=O)OC)O)[O-]
• Isomeric SMILES: CC[C@@]12CCC[N+]3([C@@H]1C4=C(CC3)C5=CC=CC=C5N4[C@](C2)(C(=O)OC)O)[O-]

Technology Process of Vincamine N-oxide

There total 1 articles about Vincamine N-oxide 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:

Reference yield: 84.8%

vincamin (1617-90-9) → (-)-vincamine N-oxide (51442-60-5,1239866-77-3)

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In chloroform;

DOI:10.1002/recl.19881070407

Reference yield:

(-)-vincamine N-oxide (51442-60-5,1239866-77-3) → vincamin (1617-90-9)

Guidance literature:

With sodium sulfite; In methanol; water; at 20 ℃; for 0.5h;

DOI:10.1016/j.bmc.2010.04.086

upstream raw materials:

vincamin

Downstream raw materials:

vincamin

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