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Lycorenine

Base Information
  • Chemical Name:Lycorenine
  • CAS No.:477-19-0
  • Molecular Formula:C18H23NO4
  • Molecular Weight:317.385
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20963901
  • Nikkaji Number:J12.378A
  • Wikidata:Q27107263
  • ChEMBL ID:CHEMBL4208558
  • Mol file:477-19-0.mol
Lycorenine

Synonyms:lycorenine

Suppliers and Price of Lycorenine
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
  • Usbiological
  • Lycorenine
  • 20mg
  • $ 490.00
  • DC Chemicals
  • Lycorenine >98%,StandardReferencesGrade
  • 20 mg
  • $ 280.00
  • Biorbyt Ltd
  • Lycorenine >98%
  • 20 mg
  • $ 569.50
  • AvaChem
  • Lycorenin
  • 10mg
  • $ 690.00
Total 29 raw suppliers
Chemical Property of Lycorenine
Chemical Property:
  • Vapor Pressure:6.23E-10mmHg at 25°C 
  • Melting Point:199-200oC 
  • Refractive Index:1.617 
  • Boiling Point:477.7 °C at 760 mmHg 
  • Flash Point:242.7 °C 
  • PSA:51.16000 
  • Density:1.28 g/cm3 
  • LogP:2.14920 
  • XLogP3:1.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:2
  • Exact Mass:317.16270821
  • Heavy Atom Count:23
  • Complexity:482
Purity/Quality:

95%-98% *data from raw suppliers

Lycorenine *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(O3)O)OC)OC
  • Isomeric SMILES:CN1CCC2=CC[C@@H]3[C@H]([C@@H]21)C4=CC(=C(C=C4[C@H](O3)O)OC)OC
  • Description An alkaloid isolated from Lycoris radiata Herb. the base crystallizes from Me2CO in rhombic prisms and has [α]20D + 149.3°. The alkaloid yields crystalline salts and derivatives, e.g. the aurichloride decomposing at 116°C, platinichloride, also decomposing before melting at 210°C; picrate, m.p. 162°C (dec.); monoacetyl derivative, m.p. 185 _7°C. The diacetyl compound has been prepared although with some difficulty and under forcing conditions, m.p. 17 5-6°C. The alkaloid behaves as a pseudo-base giving an oxime hydrochloride which decomposes at 258°C. On catalytic hydrogenation it yields the dihydro-derivative, m.p. 175- 7°C and prolonged hydrogenation eventually forms deoxytetrahydrolycorenine, ClsH2S03N, m.p. 165-8°C although other compounds are also formed at the same time, e.g. C1sH27 0 2N, m.p. l65-7°C and ClsH2S03N, m.p. l20-3°C. The methiodide decomposes when heated at 260°C and on treatment with silver oxide forms two methine bases, of which the (±)-form has been isolated as the methiodide, m.p. 223°C (dec.). The complete structure has been determined primarily from the mass spectrum.
  • Uses Lycorenine is an antibacterial agent extracted from the bulb of Lycoris radiata.
Technology Process of Lycorenine

There total 1 articles about Lycorenine 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:

Guidance literature:
Homolycorin, THF, LiAlH4, -40grad bis -50grad; neben Tetrahydro-homolycorin XI;
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