5,6,7,8,9,10-Hexahydro-5-(2-(diethylamino)ethyl)-5H-cyclohept(b)indole fumarate

Base Information

Chemical Name:5,6,7,8,9,10-Hexahydro-5-(2-(diethylamino)ethyl)-5H-cyclohept(b)indole fumarate
CAS No.:17929-92-9
Molecular Formula:C23H32N2O4
Molecular Weight:400.5112
Hs Code.:

Synonyms:5H-Cyclohept(b)indole, 5,6,7,8,9,10-hexahydro-5-(2-(diethylamino)ethyl)-, fumarate (1:1);5,6,7,8,9,10-Hexahydro-5-(2-(diethylamino)ethyl)-5H-cyclohept(b)indole fumarate;17929-92-9;C19H28N2.C4H4O4;C19-H28-N2.C4-H4-O4;LS-56221

Suppliers and Price of 5,6,7,8,9,10-Hexahydro-5-(2-(diethylamino)ethyl)-5H-cyclohept(b)indole fumarate

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 0 raw suppliers

Chemical Property of 5,6,7,8,9,10-Hexahydro-5-(2-(diethylamino)ethyl)-5H-cyclohept(b)indole fumarate

Chemical Property:

Vapor Pressure:1.35E-07mmHg at 25°C
Boiling Point:430°Cat760mmHg
Flash Point:213.8°C
Density:g/cm³
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:6
Exact Mass:400.23620751
Heavy Atom Count:29
Complexity:442

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC[NH+](CC)CCN1C2=C(CCCCC2)C3=CC=CC=C31.C(=CC(=O)[O-])C(=O)O
Isomeric SMILES:CC[NH+](CC)CCN1C2=C(CCCCC2)C3=CC=CC=C31.C(=C/C(=O)[O-])\C(=O)O

Technology Process of 5,6,7,8,9,10-Hexahydro-5-(2-(diethylamino)ethyl)-5H-cyclohept(b)indole fumarate

There total 1 articles about 5,6,7,8,9,10-Hexahydro-5-(2-(diethylamino)ethyl)-5H-cyclohept(b)indole fumarate 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: