154046-98-7

Basic information

• Product Name: (2,4-dichlorophenyl)(1H-pyrrol-2-yl)methanone
• Synonyms: (2,4-dichlorophenyl)(1H-pyrrol-2-yl)methanone
• CAS NO: 154046-98-7
• Molecular Weight: 240.089
• Mol File: 154046-98-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (2,4-dichlorophenyl)(1H-pyrrol-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (2,4-dichlorophenyl)(1H-pyrrol-2-yl)methanone(154046-98-7)
• EPA Substance Registry System: (2,4-dichlorophenyl)(1H-pyrrol-2-yl)methanone(154046-98-7)

Safety Data

• Hazardous Substances Data: 154046-98-7(Hazardous Substances Data)

Upstream product

• 109-97-7 pyrrole 
• 89-75-8 2,4-dichlorobenzoyl chloride 
• 6392-25-2 (2,4-dichlorophenyl)(morpholino)methanone 

Downstream Products

• 1528751-60-1 ethyl {2-[(2,4-dichlorophenyl)carbonyl]-1H-pyrrol-1-yl}acetate 
• 155636-03-6 (2,4-Dichloro-phenyl)-[1-((E)-3-phenyl-allyl)-1H-pyrrol-2-yl]-methanone 
• 155635-99-7 (1-Cyclopropylmethyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanone 
• 155635-91-9 (2,4-Dichloro-phenyl)-(1-propyl-1H-pyrrol-2-yl)-methanone 
• 155635-95-3 2-(2,4-dichlorobenzoyl)-1-methylpyrrole 
• 154047-04-8 (1-Allyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanone 
• 154047-17-3 (2,4-Dichloro-phenyl)-(1H-pyrrol-2-yl)-methanol 
• 944656-13-7 (2,4-Dichloro-phenyl)-(1-methyl-1H-pyrrol-2-yl)-methanol 
• 154047-23-1 (1-Allyl-1H-pyrrol-2-yl)-(2,4-dichloro-phenyl)-methanol 

Relevant articles and documents

Synthesis of a new compound family, 1-aryl-3H-pyrrolo[2,1-d][1,2,5] triazepin-4(5H)-ones

Representatives of a new family, 1-aryl-3H-pyrrolo[2,1-d][1,2,5]triazepin- 4(5H)-ones have been synthesized at our laboratory as bioisosters of biologically active 1-aryl-2,3-benzodiazepine-4-ones. The efficient synthetic route described applies the synth

Antifungal agents, II: Synthesis and antifungal activities of aryl-1H-pyrrol-2-yl-1H-imidazol-1-yl-methane derivatives with unsaturated chains

The synthesis and antifungal activities of aryl-1H-pyrrol-2-yl-1H-imidazol-1-yl-methanes having allyl, crotyl, and acrylate chains linked to the N-pyrrole atom and substituted at phenyl ring by Cl, F, CH3, and NO2 groups are reported

Process for preparing 5-aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates (I) and intermediates therefor

5-Aroyl-2,3-dihydro-1H-pyrrolizine-1,1-dicarboxylates of the formula STR1 are prepared from 2-aroylpyrroles. Hydrolysis and mono-decarboxylation of these compounds affords ketorolac and related compounds.