73177-34-1

Basic information

• Product Name: 2-ethyl-3,5-dimethyl-1H-indole
• Synonyms: 2-ethyl-3,5-dimethyl-1H-indole
• CAS NO: 73177-34-1
• Molecular Formula: C₁₂H₁₅N
• Molecular Weight: 173.2542
• Mol File: 73177-34-1.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-ethyl-3,5-dimethyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ethyl-3,5-dimethyl-1H-indole(73177-34-1)
• EPA Substance Registry System: 2-ethyl-3,5-dimethyl-1H-indole(73177-34-1)

Safety Data

• Hazardous Substances Data: 73177-34-1(Hazardous Substances Data)

Upstream product

• 100161-85-1 4-Methyl-2-((E)-1-methyl-but-2-enyl)-phenylamine 
• 583-68-6 2-bromo-p-toluidine 
• 96-22-0 pentan-3-one 
• 83191-44-0 {4-methyl-2-[(2E)-1-methylbut-2-en-1-yl]phenyl}-amine 
• 1411933-76-0 N-{4-methyl-2-[(2E)-1-methylbut-2-en-1-yl]-phenyl}-2-nitrobenzenesulfonamide 
• 110-89-4 piperidine 
• 637-60-5 p-tolylhydrazine hydrochloride 

Relevant articles and documents

Reactions of N-and C-alkenylanilines: X.* Synthesis of 2-vinyldihydroindoles from 4-methyl-2-(pent-3-en-2-yl)aniline

2-(1-Iodoethyl)-3,5-dimethyl-1-(4-methylphenylsulfonyl)-2, 3-dihydro-1H-indole reacted with pyridine, piperidine, N-alkylpiperidines, and dimethylformamide to give dehydrohalogenation and halogen substitution products whose ratio depended on the reagent s

INTRAMOLECULAR CATALYTIC CYCLIZATION OF SUBSTITUTED 2-ALKENYLANILINES

A study was carried out on the effect of the nature and structure of the substituent in the aromatic ring of 2-(1-methyl-2-butenyl)anilines on the direction and structural selectivity of the their intramolecular cyclization to derivatives of quinoline and indole by the action of catalytic amounts of PdCl2 or PdCl2-(DMSO)n complexes.