100108-66-5

Basic information

• Product Name: murrayaquinone A
• Synonyms: murrayaquinone A;3-Methyl-1H-carbazole-1,4(9H)-dione
• CAS NO: 100108-66-5
• Molecular Formula: C₁₃H₉NO₂
• Molecular Weight: 0
• Mol File: 100108-66-5.mol
• Article Data: 28

Chemical Properties

• Boiling Point: 444.8°Cat760mmHg
• Flash Point: 222.9°C
• Appearance: /
• Density: 1.38g/cm³
• Vapor Pressure: 4.17E-08mmHg at 25°C
• Refractive Index: 1.711
• CAS DataBase Reference: murrayaquinone A(CAS DataBase Reference)
• NIST Chemistry Reference: murrayaquinone A(100108-66-5)
• EPA Substance Registry System: murrayaquinone A(100108-66-5)

Safety Data

• Hazardous Substances Data: 100108-66-5(Hazardous Substances Data)

Usage

InChI:InChI=1/C13H9NO2/c1-7-6-10(15)12-11(13(7)16)8-4-2-3-5-9(8)14-12/h2-6,14H,1H3

Upstream product

• 1375488-00-8 9-benzyl-(4-benzyloxy)-1-bromo-9H-carbazole-3-carbaldehyde 
• 1375487-97-0 4-hydroxy-9H-carbazole-3-carbaldehyde 
• 1375487-98-1 4-hydroxy-9H-carbazole-1-carbaldehyde 
• 1375487-99-2 1-bromo-4-hydroxy-9H-carbazole-3-carbaldehyde 
• 1375488-02-0 (9-benzyl-1,4-dimethoxy-9H-carbazol-3-yl)methanol 
• 1384959-45-8 9-benzyl-3-(hydroxymethyl)-9H-carbazole-1,4-dione 
• 1384959-46-9 9-benzyl-3-(bromomethyl)-9H-carbazole-1,4-dione 
• 1384959-47-0 3-bromo-4-hydroxy-9H-carbazole-1-carbaldehyde 
• 1384959-48-1 9-benzyl-4-(benzyloxy)-3-bromo-9H-carbazole-1-carbaldehyde 
• 1384959-49-2 9-benzyl-4-(benzyloxy)-3-bromo-1-(1,3-dioxan-2-yl)-9H-carbazole 
• 1384959-50-5 9-benzyl-4-(benzyloxy)-1-(1,3-dioxan-2-yl)-3-methyl-9H-carbazole 
• 52602-39-8 9H-carbazol-4-ol 
• 1620580-02-0 N-(2-bromophenyl)-2,5-dimethoxy-4-methylaniline 
• 1620580-03-1 2-((2-bromophenyl)amino)-5-methylcyclohexa-2,5-diene-1,4-dione 

Relevant articles and documents

Synthesis of carbazoloquinone derivatives and their antileukemic activity via modulating cellular reactive oxygen species

Carbazoloquinone alkaloids are of great interest as privileged structures for anticancer drug molecules. The purpose of this study was to investigate the structure-activity relationships of carbazoloquinone derivatives as anticancer agents. A series of ca

Divergent Syntheses of Carbazole Alkaloids

Starting from common intermediate methyl 1-hydroxy-9 H -carbazole-3-carboxylate, synthetic routes toward murrayaquinone A, olivacine, and N -methylcalothrixin B were developed.

Concise synthesis and antiproliferative activity evaluation of ellipticine quinone and its analogs

We developed a concise protocol for the synthesis of ellipticine quinone from the appropriate 3-iodoindole-2-carbaldehydes in four steps. The key step is the construction of carbazole-1,4-quinone through tandem Ring-Closing Metathesis (RCM) and dehydrogen