9H-Carbazole-3-carbonitrile, 9-methyl-

Base Information

Chemical Name:9H-Carbazole-3-carbonitrile, 9-methyl-
CAS No.:91828-10-3
Molecular Formula:C14H10N2
Molecular Weight:206.247
Hs Code.:
DSSTox Substance ID:DTXSID60452586
Nikkaji Number:J3.081.052J
Wikidata:Q82273310

Synonyms:9-methyl-9H-carbazole-3-carbonitrile;9H-Carbazole-3-carbonitrile, 9-methyl-;9-methylcarbazole-3-carbonitrile;91828-10-3;3-cyano-9-methylcarbazole;SCHEMBL9103614;DTXSID60452586;FWJGUXCSLUENCG-UHFFFAOYSA-N

Suppliers and Price of 9H-Carbazole-3-carbonitrile, 9-methyl-

Supply Marketing:

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

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Chemical Property of 9H-Carbazole-3-carbonitrile, 9-methyl-

Chemical Property:

XLogP3:3.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:206.084398327
Heavy Atom Count:16
Complexity:316

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1C2=C(C=C(C=C2)C#N)C3=CC=CC=C31

Technology Process of 9H-Carbazole-3-carbonitrile, 9-methyl-

There total 1 articles about 9H-Carbazole-3-carbonitrile, 9-methyl- 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:

: 33268-90-5
3-chloro-9-methyl-9H-carbazole

: 151-50-8
potassium cyanide

: 1484-12-4
N-methylcarbazole

: 91828-10-3
9-methyl-9H-carbazole-3-carbonitrile

Guidance literature:: In water; tert-butyl alcohol; for 1h; Irradiation;

Reference yield:

: 91828-10-3
9-methyl-9H-carbazole-3-carbonitrile

: 521971-77-7
2-{4'-(6-methacryloyloxy-1-hexyloxy)biphenyl-4-yl}-5-(3-N-methylcarbazoyl)-1,3,4-oxadiazole

Guidance literature:: Multi-step reaction with 2 steps

1: 86 percent / sodium azide; ammonium chloride / dimethylformamide / 10 h / 140 °C

2: 62 percent / pyridine / 155 °C

With pyridine; sodium azide; ammonium chloride; In N,N-dimethyl-formamide;
DOI:10.1021/ma021406u