N-Methyl (+-)-13-alpha-hydroxyxylopinine iodide (beta)

Base Information Edit

Chemical Name:N-Methyl (+-)-13-alpha-hydroxyxylopinine iodide (beta)
CAS No.:120021-25-2
Molecular Formula:C₂₂H₂₈NO₅*I
Molecular Weight:513.373
Hs Code.:
Mol file:120021-25-2.mol

Synonyms:N-Methyl (+-)-13-alpha-hydroxyxylopinine iodide (beta);120021-25-2;6H-Dibenzo(a,g)quinolizinium, 5,8,13,13a-tetrahydro-13-hydroxy-7-methyl-2,3,10,11-tetramethoxy-, iodide, (7-alpha,13-alpha,13a-beta)-(+-)-;C22-H28-N-O5.I

Suppliers and Price of N-Methyl (+-)-13-alpha-hydroxyxylopinine iodide (beta)

Supply Marketing:Edit

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of N-Methyl (+-)-13-alpha-hydroxyxylopinine iodide (beta) Edit

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:g/cm³
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:513.10122
Heavy Atom Count:29
Complexity:547

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[N+]12CCC3=CC(=C(C=C3C1C(C4=CC(=C(C=C4C2)OC)OC)O)OC)OC.[I-]
Isomeric SMILES:C[N+]12CCC3=CC(=C(C=C3[C@@H]1[C@H](C4=CC(=C(C=C4C2)OC)OC)O)OC)OC.[I-]

Technology Process of N-Methyl (+-)-13-alpha-hydroxyxylopinine iodide (beta)

There total 2 articles about N-Methyl (+-)-13-alpha-hydroxyxylopinine iodide (beta) 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:

: 59414-58-3
trans-13-hydroxy-2,3,10,11-tetramethoxytetrahydroprotoberberine

: 74-88-4
methyl iodide

: 83527-65-5,120021-24-1,120021-25-2
13-hydroxyxylopinine methiodide

Guidance literature:: In ethanol; at 20 ℃; for 24h; Yield given;
DOI:10.1007/BF00758315

Reference yield:

: 62926-44-7
erythro (+/-)-α-hydroxylaudanosine hydrochloride

: 83527-65-5,120021-24-1,120021-25-2
13-hydroxyxylopinine methiodide

Guidance literature:: Multi-step reaction with 2 steps

1: 77 percent / ethanol; H₂O / 8 h / 20 °C

2: ethanol / 24 h / 20 °C

In ethanol; water;
DOI:10.1007/BF00758315