CAS 1484-12-4: N-Methylcarbazole
Formula:C13H11N
InChI:InChI=1S/C13H11N/c1-14-12-8-4-2-6-10(12)11-7-3-5-9-13(11)14/h2-9H,1H3
InChI key:InChIKey=SDFLTYHTFPTIGX-UHFFFAOYSA-N
SMILES:CN1C=2C(C=3C1=CC=CC3)=CC=CC2
Synonyms:- 9-methyl-9H-carbazole
- 9H-Carbazole, 9-methyl-
- Carbazole, 9-methyl-
- Methylcarbazole
- N-Methyl-9H-carbazole
- N-Methylcarbazole
- NSC 121195
- 9-Methylcarbazole
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Found 6 products.
9-Methylcarbazole
CAS:Formula:C13H11NPurity:>99.0%(GC)Color and Shape:White to Orange to Green powder to crystalMolecular weight:181.249H-Carbazole, 9-methyl-
CAS:Formula:C13H11NPurity:97%Color and Shape:SolidMolecular weight:181.233140000000029-METHYL-9H-CARBAZOLE
CAS:Purity:95.0%Color and Shape:Solid, Crystalline PowderMolecular weight:181.23800659179688N-Methylcarbazole, 99%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C13H11NPurity:99%Color and Shape:White, Crystalline powderMolecular weight:181.249-Methylcarbazole
CAS:9-Methylcarbazole belongs to the group of diphenyl sulfoxides. It is a possible metabolite of carbazole, which is used as an insecticide in agriculture and forestry. 9-Methylcarbazole is a substrate for cytochrome P450 (CYP) enzymes, catalyzing the hydroxylation of 9-methylcarbazole to form 9-hydroxymethylcarbazole. The reaction mechanism has been determined by thermodynamic data and kinetic studies. The hydrolysis of 9-methylcarbazole can be achieved with trifluoroacetic acid or sodium hydroxide in the presence of piperonyl butoxide. The basic structure consists of two amines and one phenyl ring, which are connected via a sulfoxide linkage.Purity:Min. 95%Ref: 3D-FM62361
Discontinued product
