6,11-Dihydro-5h-naphtho[2,1-a]carbazole

Base Information

Chemical Name:6,11-Dihydro-5h-naphtho[2,1-a]carbazole
CAS No.:79074-24-1
Molecular Formula:C₂₀H₁₅N
Molecular Weight:269.346
Hs Code.:
NSC Number:133078
DSSTox Substance ID:DTXSID10299827
Wikidata:Q82042496

Synonyms:79074-24-1;6,11-dihydro-5h-naphtho[2,1-a]carbazole;NSC133078;DTXSID10299827;AKOS024325670;NSC-133078

Suppliers and Price of 6,11-Dihydro-5h-naphtho[2,1-a]carbazole

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 2 raw suppliers

Chemical Property of 6,11-Dihydro-5h-naphtho[2,1-a]carbazole

Chemical Property:

Vapor Pressure:3.71E-10mmHg at 25°C
XLogP3:5.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:0
Exact Mass:269.120449483
Heavy Atom Count:21
Complexity:391

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2=C(C3=C1C4=CC=CC=C4C=C3)NC5=CC=CC=C25

Technology Process of 6,11-Dihydro-5h-naphtho[2,1-a]carbazole

There total 2 articles about 6,11-Dihydro-5h-naphtho[2,1-a]carbazole 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: 54.0%

: 573-22-8
3,4-dihydro-2H-phenanthren-1-one

: 100-63-0
phenylhydrazine

: 79074-24-1
11H-5,6-Dihydronaphtho<2,1-a>carbazole

Guidance literature:: In acetic acid; for 4h; Heating;

Reference yield:

: 781-74-8
4-(1-naphthyl)butanoic acid

: 79074-24-1
11H-5,6-Dihydronaphtho<2,1-a>carbazole

Guidance literature:: Multi-step reaction with 2 steps

1: 32 percent / PPA

2: 54 percent / acetic acid / 4 h / Heating

With PPA; In acetic acid;