246868-68-8

Basic information

• Product Name: 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2-carboxylic acid ethyl ester
• Synonyms: 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2-carboxylic acid ethyl ester
• CAS NO: 246868-68-8
• Molecular Weight: 351.402
• Mol File: 246868-68-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2-carboxylic acid ethyl ester(246868-68-8)
• EPA Substance Registry System: 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2-carboxylic acid ethyl ester(246868-68-8)

Safety Data

• Hazardous Substances Data: 246868-68-8(Hazardous Substances Data)

Upstream product

• 1041424-86-5 ethyl 4,5-di(4-methoxyphenyl)isothiazoliumbromid-2-acetate 
• 29559-26-0 (p-methoxyphenyl)nitromethane 
• 2999-46-4 Ethyl isocyanoacetate 
• 123-11-5 4-methoxy-benzaldehyde 
• 39831-04-4 1-(4-methoxyphenyl)-1-chloro-2-(4-methoxyphenyl)-2-formylethylene 
• 459-73-4 GlyOEt*HCl 
• 66521-59-3 (4-Methoxyphenyl)<1-(4-methoxyphenyl)-2-dimethylaminovinyl)>keton 
• 120-44-5 1,4-di(4-methoxyphenyl)ethanone 
• 623-33-6 glycine ethyl ester hydrochloride 

Downstream Products

• 1036356-25-8 ethyl 5-formyl-3,4-bis(4-methoxyphenyl)pyrrole-2-carboxylate 
• 1041424-88-7 3,4-di(4-methoxyphenyl)-1H-pyrrol-2-carboxylic acid 
• 2048-10-4 3,4-bis (4-methoxyphenyl)-1H-pyrrole 

Relevant articles and documents

The application of vinylogous iminium salt derivatives to a regiocontrolled and efficient relay synthesis of Lukianol A and related marine natural products

Numerous novel pyrrole containing marine natural products have been shown to possess interesting biological properties. These compounds have been the synthetic targets of several research groups and we have previously reported synthetic methods which util

Synthesis of 3,4-diaryl- and 4-acyl-3-arylpyrroles and study of their antimitotic activity

The Barton–Zard reaction of nitro substituted stilbenes and chalcones with ethyl isocyanoacetate afforded 3,4-diaryl- and 4-acyl-3-arylpyrroles, respectively. 3-Arylpyrrole-2,4- dicarboxylates and 4-arylisoxazoline N-oxides were side reaction products. An

Investigations concerning the correlation of COX-1 inhibitory and hydroxyl radical scavenging activity

The aim was to study the COX-1 inhibiting efficacy in context with hydroxyl radical scavenging properties of compounds bearing a carboxylic acid and ester function, respectively. In general, the acids are more potent radical scavengers than the corresponding esters but there is no clear correlation with their COX-1 inhibiting potencies. A feasible scavenging mechanism of carboxylic acids is discussed.