Multiflorine

Base Information

• Chemical Name: Multiflorine
• CAS No.: 529-80-6
• Molecular Formula: C₁₅H₂₂N₂O
• Molecular Weight: 246.352
• UNII: 70G8C30AVF
• Nikkaji Number: J12.718C
• Metabolomics Workbench ID: 141510
• ChEMBL ID: CHEMBL517095
• Mol file: 529-80-6.mol

Synonyms:multiflorine

Chemical Property of Multiflorine

Chemical Property:

• Vapor Pressure: 4.53E-06mmHg at 25°C
• Melting Point: 107-108 °C
• Boiling Point: 383°Cat760mmHg
• PKA: 9.17±0.20(Predicted)
• Flash Point: 165.2°C
• PSA: 23.55000
• Density: 1.19g/cm³
• LogP: 1.52350
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 246.173213330
• Heavy Atom Count: 18
• Complexity: 392

Purity/Quality:

98%min ^*data from raw suppliers

MULTIFLORINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1CCN2CC3CC(C2C1)CN4C3CC(=O)C=C4
• Isomeric SMILES: C1CCN2C[C@@H]3C[C@H]([C@@H]2C1)CN4[C@@H]3CC(=O)C=C4
• Uses: (-)-Multifluorine is a compound that is isolated from leguminous plants from the genus Lupinus.

Technology Process of Multiflorine

There total 3 articles about Multiflorine 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:

(-)-multiflorine N-oxide (137453-21-5) → (-)-multiflorine (529-80-6,10159-80-5)

Guidance literature:

With sulfur dioxide; In methanol; at 0 ℃; for 0.166667h;

Reference yield:

multiflorine → (-)-multiflorine (529-80-6) + 4α-hydroxysparteine (10349-34-5) + (-)-multiflorine (10349-35-6)

Guidance literature:

With hydrogen; Lindlar's catalyst; In ethanol; for 48h; Further Variations:; Catalysts; Product distribution;

DOI:10.1007/s007060170060

Reference yield:

→ (-)-multiflorine (529-80-6,10159-80-5)

Guidance literature:

upstream raw materials:

(-)-multiflorine N-oxide

Refernces

• 1、 Takamatsu, Satoshi,Saito, Kazuki,Ohmiya, Shigeru,Murakoshi, Isamu. "STEREOSTRUCTURE OF (-)-MULTIFLORINE N-OXIDE: A NEW LUPIN ALKALOID FROM LUPINUS HIRSUTUS". . p. 1167 - 1171. Retrieved 2007/10/02.