16498-68-3

Basic information

• Product Name: 2-Acetyl-1-methyl-1H-indole
• Synonyms: 2-Acetyl-1-methyl-1H-indole;1-(4-methyl-1H-indol-2-yl)ethanone;1-(1-METHYL-1H-INDOL-2-YL)-ETHANONE
• CAS NO: 16498-68-3
• Molecular Formula: C₁₁H₁₁NO
• Molecular Weight: 173.21
• Mol File: 16498-68-3.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Acetyl-1-methyl-1H-indole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Acetyl-1-methyl-1H-indole(16498-68-3)
• EPA Substance Registry System: 2-Acetyl-1-methyl-1H-indole(16498-68-3)

Safety Data

• Hazardous Substances Data: 16498-68-3(Hazardous Substances Data)

Usage

Physical properties

yellow to amber colored liquid with a sweet, floral odor

Common uses

fragrance ingredient in perfumes, soaps, and personal care products; synthesis of organic compounds and pharmaceuticals

Biological activities

antioxidant and anti-inflammatory properties

Safety

not fully evaluated, caution should be taken when handling and using this chemical.

Upstream product

• 13866-99-4 butane-2,3-dione-mono-(methyl-phenyl-hydrazone) 
• 60680-97-9 1-methyl-1H-indole-2-carbonitrile 
• 7647-01-0 hydrogenchloride 
• 27421-51-8 1-methyl-1H-indole-2-carboxaldehyde 
• 90965-06-3 dimethyl 1-(1-diazo-2-oxopropyl)phosphonate 
• 548489-89-0 N-methoxy-N-methyl-1-methylindole-2-carboxamide 
• 156571-69-6 N-methoxy-N-methyl-1H-indole-2-carboxamide 
• 1477-50-5 Indole-2-carboxylic acid 
• 6203-15-2 2,2,2-trifluoro-N-(2-formylphenyl)acetamide 
• 529-23-7 o-aminobenzaldehyde 
• 5344-90-1 2-Aminobenzyl alcohol 
• 4264-35-1 2-acetylindole 
• 74-88-4 methyl iodide 
• 29124-10-5 1-(1-methyl-1H-indol-2-yl)ethanol 

Downstream Products

• 127019-98-1 2-(1-methyl-1H-indol-2-yl)acetic acid 
• 1170699-72-5 (E)-4-methoxy-N-[1-(1-methyl-1H-indol-2-yl)ethylidene]aniline 
• 1620065-16-8 C₂₇H₃₄NO₃P 
• 1373438-54-0 (E)-5-bromo-2-hydroxy-4-methoxy-N'-(1-(1-methyl-1H-indol-2-yl)ethylidene)benzohydrazide 
• 1415724-51-4 C₁₉H₁₇BrN₂O₃ 
• 1415724-50-3 C₁₈H₁₅BrN₂O₃ 
• 1350889-10-9 (E/Z)-5-bromo-2-hydroxy-N'-(1-(1-methyl-1H-indol-2-yl)ethylidene)benzohydrazide 
• 1273047-11-2 (3R,7R,8S,8aR)-8-ethyl-7-[2-(1-methyl-2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine 
• 1273047-88-3 (3R,7S,8S,8aR)-8-ethyl-7-[2-(1-methyl-2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine 
• 1273047-17-8 (3R,7S,8S,8aR)-6-(benzyloxycarbonyl)-8-ethyl-7-[2-(1-methyl-2-indolyl)-2-oxoethyl]-5-oxo-3-phenyl-2,3,6,7,8,8a-hexahydro-5H-oxazolo[3,2-a]pyridine 

Relevant articles and documents

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Beta-carboline derivatives, gamma-carboline derivatives as well as preparation methods and use thereof

The invention relates to beta-carboline derivatives, gamma-carboline derivatives as well as preparation methods and use thereof. The general structural formulas of the beta-carboline derivatives and the gamma-carboline derivatives are respectively describ

Synthesis of highly substituted indene derivatives by Br?nsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols

An efficient synthetic method to prepare highly substituted indenes in moderate to excellent yields that relies on Br?nsted acid catalyzed Friedel-Crafts reaction of homoallylic alcohols under mild conditions is described.