16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3beta)-

Base Information

Chemical Name:16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3beta)-
CAS No.:115-36-6
Molecular Formula:C₁₆H₂₃NO₃
Molecular Weight:277.364
Hs Code.:
DSSTox Substance ID:DTXSID80921582
Nikkaji Number:J1.565.702B
Wikidata:Q82894520
ChEMBL ID:CHEMBL3318887
Mol file:115-36-6.mol

Synonyms:115-36-6;16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3beta)-;CHEMBL3318887;(1S,13S,16S)-16-methoxy-5-oxa-10-azatetracyclo[8.7.0.01,13.02,7]heptadec-2(7)-en-4-one;14,17-Dihydro-3-methoxy-16(15H)-oxaerythrinan-15-one (3beta)-;DTXSID80921582;BDBM50497832;16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3.beta.)-;6-Methoxy-1,4,6,7,8,8a,9,10,12,13-decahydro-3H,5H-pyrano[4',3':3,4]pyrido[2,1-i]indol-3-one

Suppliers and Price of 16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3beta)-

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

Total 6 raw suppliers

Chemical Property of 16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3beta)-

Chemical Property:

Vapor Pressure:1.03E-08mmHg at 25°C
Boiling Point:461.9°C at 760 mmHg
Flash Point:233.2°C
PSA：38.77000
Density:1.21g/cm³
LogP:1.83110
XLogP3:0.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:277.16779360
Heavy Atom Count:20
Complexity:472

Purity/Quality:: 98%,99%, ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1CCC2CCN3C2(C1)C4=C(CC3)COC(=O)C4
Isomeric SMILES:CO[C@H]1CC[C@H]2CCN3[C@]2(C1)C4=C(CC3)COC(=O)C4

Technology Process of 16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3beta)-

There total 1 articles about 16(15H)-Oxaerythrinan-15-one, 14,17-dihydro-3-methoxy-, (3beta)- 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: