885056-97-3

Basic information

• Product Name: 5-chloro-2-(1H-pyrrol-1-yl)benzaldehyde
• Synonyms: 5-chloro-2-(1H-pyrrol-1-yl)benzaldehyde
• CAS NO: 885056-97-3
• Molecular Weight: 205.644
• Mol File: 885056-97-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 5-chloro-2-(1H-pyrrol-1-yl)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 5-chloro-2-(1H-pyrrol-1-yl)benzaldehyde(885056-97-3)
• EPA Substance Registry System: 5-chloro-2-(1H-pyrrol-1-yl)benzaldehyde(885056-97-3)

Safety Data

• Hazardous Substances Data: 885056-97-3(Hazardous Substances Data)

Upstream product

• 88442-97-1 methyl 4-chloro-2-(1H-pyrrol-1-yl)benzoate 
• 5202-89-1 4-chlorobenzenesulfonyl chloride 
• 63243-75-4 ethyl 2-amino-5-chlorobenzoate 
• 885056-95-1 ethyl 5-chloro-2-(pyrrol-1-yl)benzoate 
• 885056-96-2 5-chloro-2-(pyrrol-1-yl)benzyl alcohol 

Downstream Products

• 1604835-37-1 (Z)-N-(tert-butyl)-3-chloro-9-ethyl-6-(4-methoxybenzyl)-7-oxo-6,7-dihydro-5H-benzo[b]pyrrolo[2,1-i][1,5]diazonine-5-carboxamide 
• 1604835-38-2 (Z)-N-(tert-butyl)-3-chloro-6-(4-methoxybenzyl)-9-methyl-7-oxo-6,7-dihydro-5H-benzo[b]pyrrolo[2,1-i][1,5]diazonine-5-carboxamide 
• 1604835-52-0 N-{2-(tert-butylamino)-1-[5-chloro-2-(1H-pyrrol-1-yl)phenyl]-2-oxoethyl}-N-(4-methoxybenzyl)but-2-ynamide 
• 1604835-51-9 N-{2-(tert-butylamino)-1-[5-chloro-2-(1H-pyrrol-1-yl)phenyl]-2-oxoethyl}-N-(4-methoxybenzyl)pent-2-ynamide 
• 1604835-54-2 N-{2-(butylamino)-1-[5-chloro-2-(1H-pyrrol-1-yl)phenyl]-2-oxoethyl}-N-(4-methoxybenzyl)-3-phenylpropiolamide 
• 1604835-50-8 N-(benzo[d][1,3]dioxol-5-ylmethyl)-N-{2-(tert-butylamino)-1-[5-chloro-2-(1H-pyrrol-1-yl)phenyl]-2-oxoethyl}but-2-ynamide 
• 1001053-75-3 1-(4-chloro-2-oxiranylphenyl)pyrrole 
• 941306-24-7 (6-chloro-3a-aza-cyclopenta[a]inden-8-ylidene)-phenyl-amine 

Relevant articles and documents

Regioselective synthesis of diversely substituted diazoninones through a post-Ugi gold-catalyzed intramolecular hydroarylation process

A highly efficient approach for the regioselective construction of fused nine-membered rings (diazoninone framework) was developed by employing sequential Ugi and gold-catalyzed intramolecular hydroarylation reactions. The scope of this intramolecular cyc

A facile synthesis of 9-dialkylamino-9H-pyrrolo[1,2-a]indoles via iminium salts generated from 2-(pyrrol-1-yl)benzaldehydes and secondary amine hydrochlorides in the presence of NaI/TMSCl/Et3N

The NaI/TMSCl/Et3N-mediated condensation between 2-(pyrrol-1-yl)benzaldehydes and secondary amine hydrochlorides followed by intramolecular trapping of the resulting iminium carbon by the 2-position of the pyrrole ring afforded corresponding 9-