97090-93-2

Basic information

• Product Name: 1-(4-chlorophenyl)-2-(1H-pyrrol-1-yl)ethan-1-one
• Synonyms: 1-(4-chlorophenyl)-2-(1H-pyrrol-1-yl)ethan-1-one
• CAS NO: 97090-93-2
• Molecular Weight: 219.671
• Mol File: 97090-93-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(4-chlorophenyl)-2-(1H-pyrrol-1-yl)ethan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-chlorophenyl)-2-(1H-pyrrol-1-yl)ethan-1-one(97090-93-2)
• EPA Substance Registry System: 1-(4-chlorophenyl)-2-(1H-pyrrol-1-yl)ethan-1-one(97090-93-2)

Safety Data

• Hazardous Substances Data: 97090-93-2(Hazardous Substances Data)

Upstream product

• 109-97-7 pyrrole 
• 536-38-9 4-chlorobenzoylmethyl bromide 
• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 5467-71-0 4-chlorophenacylamine hydrochloride 

Downstream Products

• 97090-86-3 1-[2-(2-Chloro-benzyloxy)-2-(4-chloro-phenyl)-ethyl]-1H-pyrrole 
• 97090-87-4 1-[2-(4-Chloro-benzyloxy)-2-(4-chloro-phenyl)-ethyl]-1H-pyrrole 
• 97210-23-6 (±)-1-(4-chlorophenyl)-2-(1H-pyrrol-1-yl)ethanol 

Relevant articles and documents

Palladium-Catalyzed Enantioselective Decarboxylative Allylic Alkylation of Acyclic α- N-Pyrrolyl/Indolyl Ketones

The synthesis of fully substituted α-N-pyrrolyl and indolyl ketones via enantioselective palladium-catalyzed allylic alkylation is described. The acyclic ketones are alkylated in high yields with high enantioselectivities through the use of an electron-deficient phosphinooxazoline ligand, furnishing a highly congested and synthetically challenging stereocenter. The obtained alkylation products contain multiple reactive sites poised for additional functionalizations and diversification.

Research on antibacterial and antifungal agents. IV. Synthesis and antifungal activity of econazole analogues with pyrrole structure

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