114049-59-1

Basic information

• Product Name: (9H-carbazol-9-yl)(2-chlorophenyl)methanone
• Synonyms: (9H-carbazol-9-yl)(2-chlorophenyl)methanone
• CAS NO: 114049-59-1
• Molecular Weight: 305.763
• Mol File: 114049-59-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (9H-carbazol-9-yl)(2-chlorophenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (9H-carbazol-9-yl)(2-chlorophenyl)methanone(114049-59-1)
• EPA Substance Registry System: (9H-carbazol-9-yl)(2-chlorophenyl)methanone(114049-59-1)

Safety Data

• Hazardous Substances Data: 114049-59-1(Hazardous Substances Data)

Upstream product

• 866594-44-7 9-(4-chloro-3-pyridinecarbonyl)carbazole 
• 866594-50-5 9-(4-bromo-3-pyridinecarbonyl)carbazole 
• 866594-45-8 9-(3-bromo-2-pyridinecarbonyl)carbazole 
• 866594-40-3 9-(3-bromo-4-pyridinecarbonyl)carbazole 
• 866594-42-5 9-(2-chloro-3-pyridinecarbonyl)carbazole 
• 86-74-8 9H-carbazole 
• 118-91-2 ortho-chlorobenzoic acid 
• 125424-72-8 (9H-carbazol-9-yl)(2-iodophenyl)methanone 
• 114049-61-5 N-(3-nitrobenzoyl)-carbazole 
• 114049-60-4 (9H-carbazol-9-yl)(4-methoxyphenyl)methanone 
• 19264-68-7 9-benzoyl-9H-carbazole 
• 73500-82-0 9-carbazole carbonyl chloride 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 609-65-4 o-chlorobenzoyl chloride 

Downstream Products

• 7469-85-4 9-(3-pyridinecarbonyl)carbazole 
• 331973-76-3 (2-bromophenyl)(9H-carbazol-9-yl)methanone 
• 19264-68-7 9-benzoyl-9H-carbazole 
• 25882-13-7 9H-indolo<3,2,1-de>phenanthridine-9-one 
• 125424-72-8 (9H-carbazol-9-yl)(2-iodophenyl)methanone 
• 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 
• 114049-60-4 (9H-carbazol-9-yl)(4-methoxyphenyl)methanone 
• 125424-73-9 9-(2-nitro-benzoyl)-carbazole 
• 125424-74-0 9-(2-aminobenzoyl)-carbazole 
• 86-74-8 9H-carbazole 
• 114049-62-6 3-(2-Chlorobenzoyl)-carbazole 

Relevant articles and documents

Insertion of arynes into carbon-halogen σ-bonds: Regioselective acylation of aromatic rings

Arynes were found to insert into carbon-halogen σ-bonds of various acid halides, enabling acyl and halogen moieties to be introduced simultaneously into adjacent positions of aromatic rings. The Royal Society of Chemistry.

A versatile route to benzocanthinones

Benzocanthinone (1) and five analogs (10, 12-15) were prepared by radical-induced cyclizations of halo N-aroyl derivatives of β-carboline and carbazole.

STUDIES ON ENAMIDES. PART- 1 : PHOTOCHEMICAL REARRANGEMENTS OF N-AROYLCARBAZOLES

The synthesis of 1- and 3-aroylcarbazoles has been achieved by the photolysis of N-aroylcarbazoles alongwith the formation of carbazole and the rearranged product ratio is wavelength dependent.