Viridiflorine

Base Information

• Chemical Name: Viridiflorine
• CAS No.: 551-57-5
• Molecular Formula: C15H27NO4
• Molecular Weight: 285.38
• UNII: 4F0407YP2J
• Nikkaji Number: J16.959E
• Wikidata: Q27259499
• Mol file: 551-57-5.mol

Synonyms:Viridiflorine;551-57-5;UNII-4F0407YP2J;4F0407YP2J;[(1R,8S)-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate;(Hexahydro-1H-pyrrolizin-1-yl)methyl 2,3-dihydroxy-2-(1-methylethyl)butanoate (1R-(1alpha-(2S*,3S*),7aalpha))-;Butanoic acid, 2,3-dihydroxy-2-(1-methylethyl)-, (hexahydro-1H-pyrrolizin-1-yl)methyl ester, (1R-(1alpha-(2S*,3S*),7aalpha))-;Viridoflorine;C15-H27-N-O4;SCHEMBL3438698;AKOS040734755;Q27259499;BUTANOIC ACID, 2,3-DIHYDROXY-2-(1-METHYLETHYL)-, (HEXAHYDRO-1H-PYRROLIZIN-1-YL)METHYL ESTER, (1R-(1.ALPHA.(2S*,3S*),7A.ALPHA.))-;BUTANOIC ACID, 2,3-DIHYDROXY-2-(1-METHYLETHYL)-, (HEXAHYDRO-1H-PYRROLIZIN-1-YL)METHYL ESTER, (1R-(1alpha(2S*,3S*),7Aalpha))-

Chemical Property of Viridiflorine

Chemical Property:

• Vapor Pressure: 1.45E-08mmHg at 25°C
• Melting Point: 102-103.5°C
• Boiling Point: 413.5°C at 760 mmHg
• Flash Point: 203.9°C
• PSA: 70.00000
• Density: 1.16g/cm³
• LogP: 0.71970
• XLogP3: 1.4
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 6
• Exact Mass: 285.19400834
• Heavy Atom Count: 20
• Complexity: 360

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C)C(C(C)O)(C(=O)OCC1CCN2C1CCC2)O
• Isomeric SMILES: C[C@@H]([C@@](C(C)C)(C(=O)OC[C@@H]1CCN2[C@H]1CCC2)O)O
• Description: A pyrrolizidine alkaloid, this base occurs in Cynoglossum viridif/orum and on crystallization from Me2CO furnishes colourless prisms. It is only sparingly soluble in Et20 but readily so in hot Me2CO, EtOH and H20. The methiodide has been prepared as colourless crystals from aqueous MeOH, m.p. 142-4°C. Alkaline hydrolysis yields trachelanthamidine and viridifloric acid. The structure given above is the most probable based upon its chemical reactions and spectroscopic characteristics.

Technology Process of Viridiflorine

There total 1 articles about Viridiflorine 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:

→ Cynaustralin (487-99-0,551-57-5,14140-18-2,17958-37-1,68473-85-8,68473-86-9,82354-33-4,82354-34-5,82374-02-5,83073-89-6)

Guidance literature:

O,O-Dibenzoyl-(+)-trachelanthsaeure-methylester 1. Lindelofidin, NaOCH3 2. H2, Pd-C;

DOI:10.1016/S0040-4020(01)82781-2

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