Flavinantine

Base Information

• Chemical Name: Flavinantine
• CAS No.: 19777-82-3
• Deprecated CAS: 412323-09-2
• Molecular Formula: C19H21NO4
• Molecular Weight: 327.3743
• DSSTox Substance ID: DTXSID70941552
• Wikidata: Q82918426
• Metabolomics Workbench ID: 136179
• ChEMBL ID: CHEMBL463084

Synonyms:flavinantine;Flavinantin;19777-82-3;(-)-Flavinantine;(1R,9R)-4-hydroxy-5,13-dimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one;5,6,8,14-Tetradehydro-3-hydroxy-2,6-dimethoxy-17-methylmorphinan-7-one;(+)-Flavinantine;CHEMBL463084;DTXSID70941552;AKOS040763413;3-Hydroxy-2,6-dimethoxy-17-methyl-5,6,8,14-tetradehydromorphinan-7-one

Chemical Property of Flavinantine

Chemical Property:

• Vapor Pressure: 1.62E-12mmHg at 25°C
• Boiling Point: 545.6°Cat760mmHg
• Flash Point: 283.8°C
• PSA: 59.00000
• Density: 1.33g/cm³
• LogP: 1.87610
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 2
• Exact Mass: 327.14705815
• Heavy Atom Count: 24
• Complexity: 613

Purity/Quality:

98.0% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)O)OC)OC
• Isomeric SMILES: CN1CC[C@]23C=C(C(=O)C=C2[C@H]1CC4=CC(=C(C=C34)O)OC)OC

Technology Process of Flavinantine

There total 1 articles about Flavinantine 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:

→ Flavinantin (19777-82-3,22324-01-2,93060-96-9)

Guidance literature:

entspr. Aminoisochinolin in 5percent-ig. H2SO4 1. NaNO2, H2O, 0-5grad 2. Bestrahlung, UV 3. NH4OH, Neutralisierung 4. CHCl3, Extrakt.;

DOI:10.1016/S0040-4020(01)91703-X

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