Lycodine

Base Information

Chemical Name:Lycodine
CAS No.:20316-18-1
Molecular Formula:C₁₆H₂₂N₂
Molecular Weight:242.364
Hs Code.:
UNII:7K0NX2M1NN
DSSTox Substance ID:DTXSID90942465
Wikidata:Q5975178
Metabolomics Workbench ID:70678
Mol file:20316-18-1.mol

Synonyms:lycodine

Suppliers and Price of Lycodine

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

Total 0 raw suppliers

Chemical Property of Lycodine

Chemical Property:

Vapor Pressure:9.51E-06mmHg at 25°C
Melting Point:118-119°
Boiling Point:372.6°Cat760mmHg
PKA:3.97, 8.08(at 25℃)
Flash Point:179.1°C
PSA：24.92000
Density:1.11g/cm³
LogP:3.20750
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:242.178298710
Heavy Atom Count:18
Complexity:329

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1CC2CC3=C(C=CC=N3)C4(C1)C2CCCN4
Isomeric SMILES:C[C@@H]1C[C@H]2CC3=C(C=CC=N3)[C@@]4(C1)[C@@H]2CCCN4
Description One of the numerous alkaloids obtained from the various Lycopodium species, this base has been found in L. annotinurn L. and L. fawcettii. It forms colourless crystals and has [α]D - 10° ± 2° (c 1.01, EtOH). One of the nitrogen atoms is present in a pyridine ring, the other being in the form of an imino group. The picrate is obtained as prisms from MeOH and has m.p. 229-233°C.

Technology Process of Lycodine

There total 41 articles about Lycodine 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: 95.0%

: 1438285-59-6
(4aR,5S,10bR,12R)-1-benzyl-12-methyl-2,3,4,4a,5,6-hexahydro-1H-5,10b-propano-1,7-phenanthroline

: 20316-18-1
(-)-lycodine

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In tetrahydrofuran; at 23 ℃; for 20h; Inert atmosphere;
DOI:10.1021/jo400695c