55540-33-5

Basic information

• Product Name: 1-(2-carboxy-4-chlorophenyl)pyrrole
• Synonyms: 1-(2-carboxy-4-chlorophenyl)pyrrole
• CAS NO: 55540-33-5
• Molecular Weight: 221.643
• Mol File: 55540-33-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1-(2-carboxy-4-chlorophenyl)pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(2-carboxy-4-chlorophenyl)pyrrole(55540-33-5)
• EPA Substance Registry System: 1-(2-carboxy-4-chlorophenyl)pyrrole(55540-33-5)

Safety Data

• Hazardous Substances Data: 55540-33-5(Hazardous Substances Data)

Upstream product

• 5044-38-2 1-(4-chlorophenyl)-1H-pyrrole 
• 124-38-9 carbon dioxide 
• 106-47-8 4-chloro-aniline 
• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 7379-35-3 4-chlorpyridine hydrochloride 
• 89-77-0 2-Amino-4-chlorobenzoic acid 
• 5202-89-1 4-chlorobenzenesulfonyl chloride 
• 635-21-2 5-chloroanthranilic acid 

Downstream Products

• 133662-35-8 5-chloro-2-(1-pyrrolyl)diazoacetophenone 
• 133662-39-2 acide 5-chloro-2-(1-pyrrolyl)phenyl acetique 
• 133662-30-3 chlorure de 5-chloro-2-(1-pyrrolyl)benzoyle 

Relevant articles and documents

Br?nsted Acid-Catalyzed Asymmetric Ring-Closing Alkylation of Inert N-substituted Pyrroles with α, β-Unsaturated Ketones

A Chiral Br?nsted acid catalyzed asymmetric intramolecular ring-closing alkylation of inert pyrroles with α, β-unsaturated ketones has been developed. This approach gave a wide range of 4-phenyl-4,5-dihydro-6H-benzo[f]pyrrolo[1,2-a]azepin-6-ones in high yields with good enantioselectivities under mild reaction conditions. (Figure presented.).

Tricyclic oxime ethers

The present invention relates to compounds of formula (I): STR1 wherein A, x, y, R1, R2 and R3 are as defined in the description. The compounds are useful for treating diseases requiring a selective serotonin reuptake site