1,4,6-Trimethyl-3-nitrocarbazole

Base Information

Chemical Name:1,4,6-Trimethyl-3-nitrocarbazole
CAS No.:188107-72-4
Molecular Formula:C15H14N2O2
Molecular Weight:254.2839
Hs Code.:
UNII:5Z8VXA8ARN
DSSTox Substance ID:DTXSID20172157
Nikkaji Number:J806.518G

Synonyms:1,4,6-Trimethyl-3-nitrocarbazole;188107-72-4;1,4,6-trimethyl-3-nitro-9H-carbazole;5Z8VXA8ARN;CCRIS 8642;3-Nitro-1,4,6-trimethyl-9H-carbazole;UNII-5Z8VXA8ARN;NIOSH/FE6277300;DTXSID20172157;9H-Carbazole, 1,4,6-trimethyl-3-nitro-;9H-Carbazole, 3-nitro-1,4,6-trimethyl-;FE62773000

Suppliers and Price of 1,4,6-Trimethyl-3-nitrocarbazole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 1,4,6-Trimethyl-3-nitrocarbazole

Chemical Property:

Vapor Pressure:1.05E-08mmHg at 25°C
Boiling Point:474.3°Cat760mmHg
Flash Point:240.6°C
Density:1.293g/cm³
XLogP3:4.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:254.105527694
Heavy Atom Count:19
Complexity:368

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC2=C(C=C1)NC3=C2C(=C(C=C3C)[N+](=O)[O-])C

Technology Process of 1,4,6-Trimethyl-3-nitrocarbazole

There total 2 articles about 1,4,6-Trimethyl-3-nitrocarbazole 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:

: 18028-56-3
1,4,6-trimethyl-9H-carbazole

: 188107-72-4
1,4,6-trimethyl-3-nitrocarbazole

Guidance literature:: With nitric acid; In acetic anhydride; at 20 ℃;
DOI:10.1002/jhet.1951

Reference yield:

: 614-96-0
5-methyl-1H-indole

: 188107-72-4
1,4,6-trimethyl-3-nitrocarbazole

Guidance literature:: Multi-step reaction with 2 steps

1: toluene-4-sulfonic acid / ethanol / Reflux

2: nitric acid / acetic anhydride / 20 °C

With nitric acid; toluene-4-sulfonic acid; In ethanol; acetic anhydride;
DOI:10.1002/jhet.1951

Reference yield:

: 188107-72-4
1,4,6-trimethyl-3-nitrocarbazole

: 3,4,5-trimethoxy-N-(1,4,6-trimethyl-9H-carbazol-3-yl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: reducing agent

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / chloroform / 16 h / 20 °C

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In chloroform;
DOI:10.1002/jhet.1951