Tetraphylline

Base Information

Chemical Name:Tetraphylline
CAS No.:482-94-0
Molecular Formula:C22H26N2O4
Molecular Weight:382.459
Hs Code.:
European Community (EC) Number:207-587-4
DSSTox Substance ID:DTXSID101317966
Nikkaji Number:J12.326I
Wikidata:Q104394709

Synonyms:Tetraphylline;11-Methoxyajmalicine;EINECS 207-587-4;482-94-0;tetraphyllin;Methyl (19alpha)-16,17-didehydro-11-methoxy-19-methyloxayohimban-16-carboxylate;NSC606024;SCHEMBL15385149;DTXSID101317966;Oxayohimban-16-carboxylic acid, 16,17-didehydro-11-methoxy-19-methyl-, methyl ester, (19alpha)-

Suppliers and Price of Tetraphylline

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 Tetraphylline

Chemical Property:

Vapor Pressure:2.83E-12mmHg at 25°C
Boiling Point:553°Cat760mmHg
Flash Point:288.3°C
Density:1.3g/cm³
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:382.18925731
Heavy Atom Count:28
Complexity:652

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=CC(=C5)OC
Isomeric SMILES:C[C@H]1[C@H]2CN3CCC4=C([C@@H]3C[C@@H]2C(=CO1)C(=O)OC)NC5=C4C=CC(=C5)OC

Technology Process of Tetraphylline

There total 1 articles about Tetraphylline 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:

: 482-94-0,482-95-1,482-96-2,13555-43-6,14883-83-1,36063-55-5,81202-53-1,132016-18-3
Raunitidin, (+/-)-3-Iso-20-allo-reserpsaeure-lacton

Guidance literature:: (+/-)-2,3-Seco-3-oxo-20-allo-reserpsaeure-lacton, 1.) POCl3, 2.) NaBH4;

Reference yield:

: 482-94-0
tetraphylline

: 62358-35-4
11-methoxy-19α-methyl-2-oxo-formosanane-16-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: tBuOCl, Et₃N / CH₂Cl₂

2: KOH

3: AcOH

With potassium hydroxide; tert-butylhypochlorite; acetic acid; triethylamine; In dichloromethane;