13169-73-8

Basic information

• Product Name: (4-fluorophenyl)(1H-pyrrol-2-yl)methanone
• Synonyms: (4-fluorophenyl)(1H-pyrrol-2-yl)methanone
• CAS NO: 13169-73-8
• Molecular Weight: 189.189
• Mol File: 13169-73-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: (4-fluorophenyl)(1H-pyrrol-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-fluorophenyl)(1H-pyrrol-2-yl)methanone(13169-73-8)
• EPA Substance Registry System: (4-fluorophenyl)(1H-pyrrol-2-yl)methanone(13169-73-8)

Safety Data

• Hazardous Substances Data: 13169-73-8(Hazardous Substances Data)

Upstream product

• 403-42-9 1-(4-fluorophenyl)ethanone 
• 403-29-2 2-bromo-4'-fluoroacetophenone 
• 109-97-7 pyrrole 
• 2251-76-5 2-(4-fluorophenyl)-2-oxoacetic acid 
• 403-43-0 4-fluorobenzoyl chloride 
• 20671-52-7 lithium pyrrolide 
• 459-57-4 4-fluorobenzaldehyde 
• 403-33-8 methyl 4-flurobenzoate 
• 1978-65-0 4-(4-fluorobenzoyl)morpholine 

Downstream Products

• 1528751-50-9 ethyl {2-[(4-fluorophenyl)carbonyl]-1H-pyrrol-1-yl}acetate 
• 129237-21-4 [1-(2-Chloromethyl-benzyl)-1H-pyrrol-2-yl]-(4-fluoro-phenyl)-methanone 
• 129055-81-8 (1-{2-[2-(4-Fluoro-benzoyl)-pyrrol-1-ylmethyl]-benzyl}-1H-pyrrol-2-yl)-(4-fluoro-phenyl)-methanone 
• 129055-86-3 11-(4-Fluoro-phenyl)-5H-benzo[e]pyrrolo[1,2-a]azepine 
• 154047-20-8 (1-Allyl-1H-pyrrol-2-yl)-(4-fluoro-phenyl)-methanol 
• 154047-01-5 (1-Allyl-1H-pyrrol-2-yl)-(4-fluoro-phenyl)-methanone 

Relevant articles and documents

Synthesis method of 2-aromatic acyl pyrrole compounds

The invention relates to the field of organic synthesis, and discloses a synthesis method of 2-aromatic acyl pyrrole compounds, wherein the synthesis method comprises the steps: taking an N-aromatic acyl pyrrole compound as a raw material, and carrying ou

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

A novel one-pot synthesis of 2-benzoylpyrroles from benzaldehydes

We herein report a novel one-pot reaction for benzoylation of pyrrole. The key step in the reaction is generation of di(1H-pyrrol-1-yl)zirconium(IV) chloride complex which reacts with benzaldehydes and methyl benzoates to give 2-benzoylpyrroles as the major product.