Sophoranol

Base Information

Chemical Name:Sophoranol
CAS No.:3411-37-8
Molecular Formula:C15H24N2O2
Molecular Weight:264.36326
Hs Code.:
ChEMBL ID:CHEMBL3590537
Metabolomics Workbench ID:132478
Nikkaji Number:J359.362B
Wikidata:Q27151403
Mol file:3411-37-8.mol

Synonyms:Sophoranol;3411-37-8;(+)-Sophoranol;5-Hydroxymatrine;(7AR,13aR,13bR,13cR)-dodecahydro-7a-hydroxy-1H,5H,10H-dipyrido[2,1-f:3 inverted exclamation marka,2 inverted exclamation marka,1 inverted exclamation marka-ij][1,6]naphthyridin-10-one;SCHEMBL564487;CHEMBL3590537;CHEBI:80905;AKOS040760715;FS-8019;HY-126033;CS-0090291;C17069;Q27151403;(1R,2R,9R,17R)-9-hydroxy-7,13-diazatetracyclo[7.7.1.0?,?.0??,??]heptadecan-6-one

Suppliers and Price of Sophoranol

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

TRC
5-Hydroxymatrine
10mg
$ 195.00

TRC
5-Hydroxymatrine
100mg
$ 1540.00

Arctom
(+)-Sophoranol
5mg
$ 418.00

Total 16 raw suppliers

Chemical Property of Sophoranol

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:169-170 °C
Refractive Index:1.607
Boiling Point:437.642 °C at 760 mmHg
PKA:14.05±0.20(Predicted)
Flash Point:218.478 °C
PSA：43.78000
Density:1.255 g/cm³
LogP:0.86240
XLogP3:0.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:264.183778013
Heavy Atom Count:19
Complexity:400

Purity/Quality:

99%, ^*data from raw suppliers

5-Hydroxymatrine ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2C3CCCN4C3C(CCC4)(CN2C(=O)C1)O
Isomeric SMILES:C1C[C@@H]2[C@H]3CCCN4[C@H]3[C@@](CCC4)(CN2C(=O)C1)O
Uses 5-Hydroxymatrineis an alkaloid isolated from Chines Sophorae radix and Sophora tomentosa L..

Technology Process of Sophoranol

There total 6 articles about Sophoranol 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:

: 16100-95-1
5-hydroxy-6,7-didehydro-matridin-15-one

: 3411-37-8
(+)-sophoranol

Guidance literature:: With methanol; platinum; Hydrogenation;

Reference yield:

: 16100-95-1
5-hydroxy-6,7-didehydro-matridin-15-one

: 3411-37-8,56142-59-7,109717-34-2
5-hydroxy-6β,7β-matridin-15-one

Guidance literature:: With methanol; platinum; Hydrogenation;

Reference yield:

: 641-39-4
(+)-allomatrine

: 3411-37-8
(+)-sophoranol

Guidance literature:: Multi-step reaction with 2 steps

1: mercury (II)-acetate; aqueous acetic acid

2: platinum; methanol / Hydrogenation

With methanol; mercury(II) diacetate; acetic acid; platinum;