1484-05-5

Basic information

• Product Name: 1-(9-Methyl-9H-carbazol-3-yl)-ethanone
• Synonyms: 3-Acetyl-9-methyl-9H-carbazole;1-(9-methylcarbazol-3-yl)ethanone
• CAS NO: 1484-05-5
• Molecular Formula: C₁₅H₁₃NO
• Molecular Weight: 223.27
• Mol File: 1484-05-5.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 338.9°Cat760mmHg
• Flash Point: 158.7°C
• Appearance: /
• Density: 1.14g/cm³
• Vapor Pressure: 9.54E-05mmHg at 25°C
• Refractive Index: 1.62
• CAS DataBase Reference: 1-(9-Methyl-9H-carbazol-3-yl)-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(9-Methyl-9H-carbazol-3-yl)-ethanone(1484-05-5)
• EPA Substance Registry System: 1-(9-Methyl-9H-carbazol-3-yl)-ethanone(1484-05-5)

Safety Data

• Hazardous Substances Data: 1484-05-5(Hazardous Substances Data)

Usage

General Description

1-(9-Methyl-9H-carbazol-3-yl)-ethanone is a chemical compound with the molecular formula C16H13NO. It is a carbazole derivative with a ketone functional group attached to the carbazole ring. 1-(9-Methyl-9H-carbazol-3-yl)-ethanone has a yellow-brown appearance and is soluble in organic solvents such as dichloromethane and ethyl acetate. It is commonly used as a building block in the synthesis of organic compounds and has applications in the field of chemistry and materials science. 1-(9-Methyl-9H-carbazol-3-yl)-ethanone may also have potential uses in pharmaceutical research due to its unique structure and properties.

InChI:InChI=1/C15H13NO/c1-10(17)11-7-8-15-13(9-11)12-5-3-4-6-14(12)16(15)2/h3-9H,1-2H3

Upstream product

• 1484-12-4 N-methylcarbazole 
• 75-36-5 acetyl chloride 
• 86-74-8 9H-carbazole 
• 38292-40-9 1,2-dimethyl-1H-indole-3-carbaldehyde 
• 78-94-4 methyl vinyl ketone 
• 3215-37-0 3-acetylcarbazole 
• 77-78-1 dimethyl sulfate 
• 574-39-0 9-acetylcarbazole 
• 108-24-7 acetic anhydride 

Downstream Products

• 1449676-63-4 4-methyl-N′-(1-(9-methyl-9H-carbazol-3-yl)ethylidene)benzenesulfonohydrazide 
• 1372602-87-3 3-(1-(4-(4-tert-butylphenyl)-1H-1,2,3-triazol-1-yl)ethyl)-9-methyl-9H-carbazole 
• 1372602-86-2 9-methyl-3-(1-(4-(2-nitrophenyl)-1H-1,2,3-triazol-1-yl)ethyl)-9Hcarbazole 
• 1372602-85-1 3-(1-(4-(benzyloxymethyl)-1H-1,2,3-triazol-1-yl)ethyl)-9-methyl-9H-carbazole 
• 1372602-80-6 9-methyl-3-(1-(4-phenyl-1H-1,2,3-triazol-1-yl)ethyl)-9H-carbazole 

Relevant articles and documents

Anionic Cycloaddition Reactions Of Indole-2,3-dienolate With Dienophiles: A Facile Regiospecific Route To Substituted Carbazoles

Indole 2,3-dienolate derived by deprotonation of 1,2-dimethylindole-3-carboxaldehyde is shown to be useful 1,4-dipole synthon (anionic indolo-2,3-quinodimethane) which undergoes facile cycloaddition with wide range of dienophiles affording substituted car

A Green Synthesis of 2-Amino-4-(9H-carbazole-3-yl)thiophene-3-carbonitriles by a Step-wise and One-pot Three-component Gewald Reaction

An eco-friendly method has been developed for the synthesis of 2-amino-4-(9H-carbazole-3-yl)thiophene-3-carbonitriles from preliminary carbazole (1) through an intermediate of 2-(1-(9H-carbazole-3-yl)ethylidene)malononitriles using the Knoevenagel condensation followed by the Gewald reaction. On the other hand, the target compounds could also be prepared in a one-pot three-component manner by treating equimolar quantities of 1-(9H-carbazole-3-yl)ethanone (3), malononitrile, and elemental sulfur. The merits of this preparation are mild reaction conditions. The Gewald reaction is executed with inorganic base NaHCO3 (H2O) in tetrahydrofuran, easy work-up procedure with good yields.

Design, synthesis, and structure-activity correlations of novel dibenzo[b,d furan, dibenzo[b,d]thiophene, and N-methylcarbazole clubbed 1,2,3-triazoles as potent inhibitors of mycobacterium tuberculosis

A molecular hybridization approach is an emerging structural modification tool to design new molecules with improved pharmacophoric properties. In this study, 1,2,3-triazole-based Mycobacterium tuberculosis inhibitors and synthetic and natural product-bas