Vobasan-17-oic acid, 3-oxo-, methyl ester

Base Information Edit

Chemical Name:Vobasan-17-oic acid, 3-oxo-, methyl ester
CAS No.:2134-83-0
Molecular Formula:C₂₁H₂₄N₂O₃
Molecular Weight:352.433
Hs Code.:
Wikipedia:Vobasine
Mol file:2134-83-0.mol

Synonyms:vobasine;vobasine hydrochloride;vobasine monohydrochloride

Suppliers and Price of Vobasan-17-oic acid, 3-oxo-, methyl ester

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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Total 4 raw suppliers

Chemical Property of Vobasan-17-oic acid, 3-oxo-, methyl ester Edit

Chemical Property:

Vapor Pressure:3.46E-11mmHg at 25°C
Melting Point:111-113 °C
Boiling Point:526.8°Cat760mmHg
PKA:14.95±0.40(Predicted)
Flash Point:272.4°C
PSA：62.40000
Density:1.255g/cm³
LogP:2.90040
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:352.17869263
Heavy Atom Count:26
Complexity:616

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC=C1CN(C2CC3=C(C(=O)CC1C2C(=O)OC)NC4=CC=CC=C34)C
Isomeric SMILES:C/C=C\1/CN([C@H]2CC3=C(C(=O)C[C@@H]1C2C(=O)OC)NC4=CC=CC=C34)C
Description A further alkaloid occurring in Voacanga africana, the base forms cubic crystals from MeOH and is strongly laevorotatory with [α]23D- 158.5° (c 1.0, CHCI3) or - 148.3° (c 1.0, MeOH). The ultraviolet spectrum has two absorption maxima at 239 and 315 mμ. The alkaloid forms a hydrochloride as prismatic plates from MeOH, m.p. 245-8°C (dec.); [α]22D - 120.1° (c 1.0, MeOH); the methiodide, m.p. 212-4°C (dec.); [α]23D - 117.2° (c 1.0, MeOH) and the 2:4-dinitrophenylhydrazone as deep red crystals, m.p. 172-5°C.

Technology Process of Vobasan-17-oic acid, 3-oxo-, methyl ester

There total 5 articles about Vobasan-17-oic acid, 3-oxo-, methyl ester 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: