Lamellarin T

Base Information

Chemical Name:Lamellarin T
CAS No.:189083-78-1
Molecular Formula:C30H27NO9
Molecular Weight:545.5367
Hs Code.:
DSSTox Substance ID:DTXSID90172301
Nikkaji Number:J831.359H
Wikidata:Q83042412
Metabolomics Workbench ID:143996
ChEMBL ID:CHEMBL57138

Synonyms:lamellarin T

Suppliers and Price of Lamellarin T

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 T

Chemical Property:

Boiling Point:834.3°Cat760mmHg
Flash Point:458.4°C
Density:1.43g/cm³
XLogP3:4.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:9
Rotatable Bond Count:6
Exact Mass:545.16858144
Heavy Atom Count:40
Complexity:906

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)OC)OC)OC)O

Technology Process of Lamellarin T

There total 13 articles about Lamellarin T 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: 89.0%

: 3-Isopropoxy-13-(3-isopropoxy-4-methoxy-phenyl)-2,9,10,11-tetramethoxy-7,8-dihydro-5-oxa-6b-aza-dibenzo[a,i]fluoren-6-one

: 189083-78-1
Lamellarin T

Guidance literature:: With aluminium trichloride; In dichloromethane; for 2h; Ambient temperature;
DOI:10.1021/jo9808526

Reference yield:

: 919082-26-1
1-(3-benzyloxy-4-methoxy-benzyl)-5,6,7-trimethoxy-3,4-dihydro-isoquinoline

: 189083-78-1
Lamellarin T

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

Reference yield:

: 919082-33-0
ethyl 1-(3-benzyloxy-4-methoxyphenyl)-2-(2,4-dibenzyloxy-5-methoxyphenyl)-7,8,9-trimethoxy-5,6-dihydropyrrolo[2,1-a]isoquinoline-3-carboxylate

: 189083-78-1
Lamellarin T

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