74470-85-2

Basic information

• Product Name: 2,3,3-Trimethyl-3H-benzo[g]indole
• Synonyms: 2,3,3-TRIMETHYL-3H-BENZ[G]INDOL;2,3,3-TRIMETHYL-3H-BENZ[G]INDOLE;2,3,3-TRIMETHYL-3H-BENZO[G]INDOLE;2,3,3-Trimethyl-6,7-benzoindolenine;AKOS BBS-00006364;TMBI[g];2,3,3-Trimethyl-6,7-benzoindolenine/TMBI[g];2,3,3-Trimethylnaphtho[1,2-b]pyrrole
• CAS NO: 74470-85-2
• Molecular Formula: C₁₅H₁₅N
• Molecular Weight: 209.29
• Product Categories: Heterocycle-Indole series
• Mol File: 74470-85-2.mol
• Article Data: 3

Chemical Properties

• Melting Point: 78 °C
• Boiling Point: 334°C
• Flash Point: 148°C
• Appearance: /
• Density: 1.06
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.6
• Storage Temp.: 2-8°C
• PKA: 5.96±0.40(Predicted)
• CAS DataBase Reference: 2,3,3-Trimethyl-3H-benzo[g]indole(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,3-Trimethyl-3H-benzo[g]indole(74470-85-2)
• EPA Substance Registry System: 2,3,3-Trimethyl-3H-benzo[g]indole(74470-85-2)

Safety Data

• Hazardous Substances Data: 74470-85-2(Hazardous Substances Data)

Usage

General Description

2,3,3-Trimethyl-3H-benzo[g]indole is a chemical compound with the molecular formula C15H15N. It is a polycyclic aromatic hydrocarbon with a tricyclic core structure. 2,3,3-Trimethyl-3H-benzo[g]indole is a derivative of indole and is commonly used in organic synthesis and pharmaceutical research. It exhibits photophysical properties and has been studied for its potential applications in light-emitting devices and fluorescent probes. Additionally, 2,3,3-Trimethyl-3H-benzo[g]indole has been investigated for its potential pharmacological activities, including its role as an inhibitor of mitochondrial complex I and its potential use as an antineoplastic agent. Overall, this compound has shown promise in various research fields and continues to be of interest for its versatile properties.

InChI:InChI=1/C15H15N/c1-10-15(2,3)13-9-8-11-6-4-5-7-12(11)14(13)16-10/h4-9H,1-3H3

Upstream product

• 563-80-4 3-methyl-butan-2-one 
• 2243-55-2 1-(1-naphthyl)hydrazine 
• 2243-56-3 1-naphthylhydrazine hydrochloride 
• 134-32-7 1-amino-naphthalene 
• 4437-80-3 4,4-dimethyl-5-methylene-1,3-dioxolan-2-one 
• 74470-80-7 5,5-dimethyl-4-methylene-3-(naphthalen-1-yl)oxazolidin-2-one 

Downstream Products

• 58464-25-8 1,1,2,3-tetramethyl-1H-benz[e]indol-3-ium iodide 

Relevant articles and documents

Ring transformations of heterocyclic compounds. XXII [1]. Pyrido[1,2-a]indolium salts from 2-methyl-3H-indoles by pyrylium mediated three carbon annelation

The synthesis of pyrido[1,2-a]indolium perchlorates 8,11 from 2,4,6-triarylpyrylium perchlorates 1 and 2-methyl-3H-indoles 6,9 in the presence of a basic condensing agent (anhydrous sodium acetate, piperidine acetate, triethylamine/acetic acid, triethylamine) in ethanol by a 2,4-[C3+C2N] pyrylium ring transformation is reported. Spectroscopic data of the transformation products and their mode of formation are discussed.

Eine einfache Synthese von 3H-Indolen ausgehend von acetylenischen Alkoholen

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