Lamellarin E

Base Information

Chemical Name:Lamellarin E
CAS No.:115982-19-9
Molecular Formula:C29H25 N O9
Molecular Weight:531.5101
Hs Code.:
DSSTox Substance ID:DTXSID60151249
Nikkaji Number:J1.110.351K
Wikidata:Q83017675
Metabolomics Workbench ID:143877
ChEMBL ID:CHEMBL2334355
Mol file:115982-19-9.mol

Synonyms:Lamellarin E;Lamellarine E;115982-19-9;CHEMBL2334355;3,10-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,11,12-trimethoxy-8,9-dihydro-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one;6H-(1)Benzopyrano(4',3':4,5)pyrrolo(2,1-a)isoquinolin-6-one, 8,9-dihydro-3,10-dihydroxy-14-(3-hydroxy-4-methoxyphenyl)-2,11,12-trimethoxy-;DTXSID60151249;BDBM50428425;C29-H25-N-O9;AKOS040746983;7,18-dihydroxy-12-(3-hydroxy-4-methoxyphenyl)-8,16,17-trimethoxy-4-oxa-1-azapentacyclo[11.8.0.02,11.05,10.014,19]henicosa-2(11),5,7,9,12,14,16,18-octaen-3-one

Suppliers and Price of Lamellarin E

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
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price

Total 0 raw suppliers

Chemical Property of Lamellarin E

Chemical Property:

Boiling Point:847.8°Cat760mmHg
Flash Point:466.5°C
PSA：132.75000
Density:1.49g/cm³
LogP:4.78900
XLogP3:4.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:5
Exact Mass:531.15293138
Heavy Atom Count:39
Complexity:891

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C(C=C1)C2=C3C4=CC(=C(C(=C4CCN3C5=C2C6=CC(=C(C=C6OC5=O)O)OC)O)OC)OC)O

Technology Process of Lamellarin E

There total 15 articles about Lamellarin E 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:

: 121-33-5,8014-42-4
vanillin

: 115982-19-9
14-(3-hydroxy-4-methoxyphenyl)-3,10-dihydroxy-2,11,12-trimethoxy-8,9-dihydro-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one

Guidance literature:: Multi-step reaction with 4 steps

2: sodium hydrogencarbonate / acetonitrile / 18 h / Heating

3: hydrogen / palladium on activated charcoal / ethyl acetate / 20 °C / 3878.61 Torr

4: sodium hydride / tetrahydrofuran / 0 - 20 °C

With hydrogen; sodium hydride; sodium hydrogencarbonate; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate; acetonitrile;
DOI:10.1021/jo061810h

Reference yield:

: 919082-35-2
ethyl 1-(3-benzyloxy-4-methoxyphenyl)-2-(2,4-dibenzyloxy-5-methoxyphenyl)-7-benzyloxy-8,9-dimethoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carboxylate

: 115982-19-9
14-(3-hydroxy-4-methoxyphenyl)-3,10-dihydroxy-2,11,12-trimethoxy-8,9-dihydro-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium on activated charcoal / ethyl acetate / 20 °C / 3878.61 Torr

2: sodium hydride / tetrahydrofuran / 0 - 20 °C

With hydrogen; sodium hydride; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/jo061810h

Reference yield:

: 47811-27-8
5-benzyloxy-1-(3-benzyloxy-4-methoxy-benzyl)-6,7-dimethoxy-3,4-dihydro-isoquinoline

: 115982-19-9
14-(3-hydroxy-4-methoxyphenyl)-3,10-dihydroxy-2,11,12-trimethoxy-8,9-dihydro-6H-chromeno[4',3':4,5]pyrrolo[2,1-a]isoquinolin-6-one

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydrogencarbonate / acetonitrile / 18 h / Heating

2: hydrogen / palladium on activated charcoal / ethyl acetate / 20 °C / 3878.61 Torr

3: sodium hydride / tetrahydrofuran / 0 - 20 °C

With hydrogen; sodium hydride; sodium hydrogencarbonate; palladium on activated charcoal; In tetrahydrofuran; ethyl acetate; acetonitrile;
DOI:10.1021/jo061810h