1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide

Base Information

Chemical Name:1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide
CAS No.:67242-61-9
Molecular Formula:C13H14N2O
Molecular Weight:214.2631
Hs Code.:
DSSTox Substance ID:DTXSID80217578
Wikidata:Q83094134

Synonyms:1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide;67242-61-9;1,2,3,4-tetrahydrocarbazole-9-carboxamide;SCHEMBL3137735;DTXSID80217578

Suppliers and Price of 1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide

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 3 raw suppliers

Chemical Property of 1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide

Chemical Property:

Vapor Pressure:1.25E-07mmHg at 25°C
Boiling Point:430.9°Cat760mmHg
Flash Point:214.4°C
Density:1.32g/cm³
XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:214.110613074
Heavy Atom Count:16
Complexity:292

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC2=C(C1)C3=CC=CC=C3N2C(=O)N

Technology Process of 1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide

There total 2 articles about 1,2,3,4-Tetrahydro-9H-carbazole-9-carboxamide 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:

: 1189-71-5
isocyanate de chlorosulfonyle

: 942-01-8
1,2,3,4-tetrahydrocarbazole

: 67242-61-9
1,2,3,4-tetrahydrocarbazole-9-carboxamide

Guidance literature:: Yield given. Multistep reaction; 1.) benzene, ice-cooling, 0.5 h, r.t., 1 h, 2.) CH₃CN, pH 8, r.t., 12 h;
DOI:10.1248/cpb.31.423