647864-38-8

Basic information

• Product Name: 1H-Pyrrole-3-carboxylic acid, 5-[2-hydroxy-1-[(4-methylphenyl)sulfonyl]-2-(3,4,5-trimethoxyphenyl)ethyl ]-1-(methoxymethyl)-, methyl ester
• CAS NO: 647864-38-8
• Molecular Formula: C26H31NO9S
• Molecular Weight: 533.599
• Mol File: 647864-38-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole-3-carboxylic acid, 5-[2-hydroxy-1-[(4-methylphenyl)sulfonyl]-2-(3,4,5-trimethoxyphenyl)ethyl ]-1-(methoxymethyl)-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole-3-carboxylic acid, 5-[2-hydroxy-1-[(4-methylphenyl)sulfonyl]-2-(3,4,5-trimethoxyphenyl)ethyl ]-1-(methoxymethyl)-, methyl ester(647864-38-8)
• EPA Substance Registry System: 1H-Pyrrole-3-carboxylic acid, 5-[2-hydroxy-1-[(4-methylphenyl)sulfonyl]-2-(3,4,5-trimethoxyphenyl)ethyl ]-1-(methoxymethyl)-, methyl ester(647864-38-8)

Safety Data

• Hazardous Substances Data: 647864-38-8(Hazardous Substances Data)

Usage

Molecular structure

1H-Pyrrole-3-carboxylic acid, 5-[2-hydroxy-1-[(4-methylphenyl)sulfonyl]-2-(3,4,5-trimethoxyphenyl)ethyl]-1-(methoxymethyl)-, methyl ester is a complex organic compound that contains a pyrrole ring and a carboxylic acid group.

Functional groups

The compound has a methyl ester and a sulfonyl moiety, as well as hydroxy and methoxy substituents on a phenyl ring.

Potential pharmacological properties

Due to its diverse functional groups, the compound is likely to have a range of pharmacological properties.

Potential applications

The compound could potentially be used in drug development or as a research tool in the fields of medicinal chemistry and pharmacology.

Further studies needed

The exact properties and potential uses of the compound would need to be determined through additional studies and experimentation.

Upstream product

• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 155345-18-9 methyl 1-methoxymethyl-5-tosylmethyl-1H-pyrrole-3-carboxylate 

Downstream Products

• 155474-10-5 methyl N-methoxymethyl-2-[2-oxo-2-(3,4,5-trimethoxyphenyl)-1-tosylethyl]pyrrole-4-carboxylate 
• 647864-39-9 methyl N-methoxymethyl-2-[2-tosyloxy-(3,4,5-trimethoxyphenyl)-1-tosylethenyl]pyrrole-4-carboxylate 

Relevant articles and documents

Preparation of phenanthrenes by photocyclization of stilbenes containing a tosyl group on the central double bond. A versatile approach to the synthesis of phenanthrenes and phenanthrenoids

We have developed a useful modification of the classical preparation of phenanthrenes by UV irradiation of stilbenes in the presence of an oxidant. This modification involves the irradiation, in the presence of base, of stilbenes possessing a sulfonyl group linked to the central double bond. We have proved that this protocol can be successfully applied for the synthesis of diverse phenanthrenes and phenanthrenoids.

Base-Induced Photocyclization of 1,2-Diaryl-1-tosylethenes. A Mechanistically Novel Approach to Phenanthrenes and Phenanthrenoids

(Equation presented) The irradiation with UV light of a number of 1,2-diaryl-1-tosylstilbenes, in the presence of base, leads to the corresponding phenanthrenes and heterocyclic analogues. These results are consistent with a mechanism involving the base-induced elimination of p-toluenesulfinic acid from an intermediate 9-tosyl-4a,4b-dihydrophenanthrene, formed by photochemical cyclization of the starting 1,2-diaryl-1-tosylstilbenes.