125424-72-8

Basic information

• Product Name: (9H-carbazol-9-yl)(2-iodophenyl)methanone
• Synonyms: (9H-carbazol-9-yl)(2-iodophenyl)methanone
• CAS NO: 125424-72-8
• Molecular Weight: 397.215
• Mol File: 125424-72-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (9H-carbazol-9-yl)(2-iodophenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (9H-carbazol-9-yl)(2-iodophenyl)methanone(125424-72-8)
• EPA Substance Registry System: (9H-carbazol-9-yl)(2-iodophenyl)methanone(125424-72-8)

Safety Data

• Hazardous Substances Data: 125424-72-8(Hazardous Substances Data)

Upstream product

• 609-67-6 2-Iodobenzoyl chloride 
• 86-74-8 9H-carbazole 
• 866594-42-5 9-(2-chloro-3-pyridinecarbonyl)carbazole 
• 866594-40-3 9-(3-bromo-4-pyridinecarbonyl)carbazole 
• 866594-45-8 9-(3-bromo-2-pyridinecarbonyl)carbazole 
• 866594-50-5 9-(4-bromo-3-pyridinecarbonyl)carbazole 
• 866594-44-7 9-(4-chloro-3-pyridinecarbonyl)carbazole 
• 19264-68-7 9-benzoyl-9H-carbazole 
• 114049-59-1 (9H-carbazol-9-yl)(2-chlorophenyl)methanone 
• 114049-60-4 (9H-carbazol-9-yl)(4-methoxyphenyl)methanone 
• 114049-61-5 N-(3-nitrobenzoyl)-carbazole 
• 88-67-5 2-Iodobenzoic acid 

Downstream Products

• 114049-64-8 3-(3-nitrobenzoyl)-carbazole 
• 114049-61-5 N-(3-nitrobenzoyl)-carbazole 
• 114049-63-7 3-(4-Methoxybenzoyl)-carbazole 
• 114049-66-0 1-(4-Methoxybenzoyl)-carbazole 
• 114049-65-9 1-(2-Chlorobenzoyl)-carbazole 
• 114049-60-4 (9H-carbazol-9-yl)(4-methoxyphenyl)methanone 
• 114049-62-6 3-(2-Chlorobenzoyl)-carbazole 
• 114049-59-1 (9H-carbazol-9-yl)(2-chlorophenyl)methanone 
• 125424-73-9 9-(2-nitro-benzoyl)-carbazole 
• 125424-74-0 9-(2-aminobenzoyl)-carbazole 
• 19264-68-7 9-benzoyl-9H-carbazole 
• 25882-13-7 9H-indolo<3,2,1-de>phenanthridine-9-one 
• 86-74-8 9H-carbazole 

Relevant articles and documents

TFAA/H3PO4 mediated unprecedented N-acylation of carbazoles leading to small molecules possessing anti-proliferative activities against cancer cells

For the first time TFAA/H3PO4 has facilitated the direct and metal-free N-acylation of carbazoles leading to a number of N-acylated derivatives. Several of these compounds were found to be promising when tested for their anti-proliferative properties against oral cancer cell lines. This journal is the Partner Organisations 2014.

STUDIES ON ENAMIDES PART-2 : A NOVEL PHOTOCHEMICAL SYNTHESIS OF 9H-INDOLOPHENANTHRIDIN-9-ONE, A BENZCANTHINE ANALOGUE

The synthesis of 3-aroylcarbazoles and the unknown 1-aroylcarbazoles has been achieved by the photolysis of 9-aroylcarbazoles in polar solvent.Irradiation of 3(a-c) in non-polar solvent afforded regiospecifically 5(a-c), carbazole (1) and for the first time, 9H-indolophenanthridin-9-one (8) from 3b.The yield of 8 was significantly improved by UV exposure of 9-(2-iodobenzoyl)-carbazole (3e) in methanol and iodine, without providing any photomigrated product.