1169610-77-8

Basic information

• Product Name: 1-(4-bromo-2-nitrophenyl)-1H-pyrrole
• Synonyms: 1-(4-bromo-2-nitrophenyl)-1H-pyrrole
• CAS NO: 1169610-77-8
• Molecular Weight: 267.082
• Mol File: 1169610-77-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-(4-bromo-2-nitrophenyl)-1H-pyrrole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-bromo-2-nitrophenyl)-1H-pyrrole(1169610-77-8)
• EPA Substance Registry System: 1-(4-bromo-2-nitrophenyl)-1H-pyrrole(1169610-77-8)

Safety Data

• Hazardous Substances Data: 1169610-77-8(Hazardous Substances Data)

Upstream product

• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 875-51-4 4-Bromo-2-nitroaniline 

Downstream Products

• 1448531-48-3 7-[2-(3-aminophenyl)ethynyl]pyrrolo[1,2-a]quinoxaline-4-carboxylic acid 
• 1448531-80-3 ethyl 7-[2-(3-aminophenyl)ethynyl]pyrrolo[1,2-a]quinoxaline-4-carboxylate 
• 1448531-79-0 ethyl 7-[(3-ethynylphenyl)amino]pyrrolo[1,2-a]quinoxaline-4-carboxylate 
• 1448531-77-8 ethyl 2-[(5-bromo-2-pyrrolo-1-ylphenyl)amino]-2-oxoacetate 
• 896429-82-6 5-bromo-2-(1H-pyrrol-1-yl)aniline 
• 1448531-45-0 7-[(3-ethynylphenyl)amino]pyrrolo[1,2-a]quinoxaline-4-carboxylic acid 
• 1448531-44-9 7-[(3-chlorophenyl)amino]pyrrolo[1,2-a]quinoxaline-4-carboxylic acid 
• 1448531-74-5 ethyl 7-{[3-(2-trimethylsilylethynyl)phenyl]amino}pyrrolo[1,2-a]quinoxaline-4-carboxylate 
• 1448531-73-4 ethyl 7-[(3-chlorophenyl)amino]pyrrolo[1,2-a]quinoxaline-4-carboxylate 

Relevant articles and documents

TFAA-Catalyzed Annulation Synthesis of Spiro Pyrrolo[1,2-a]quinoxaline Derivatives from 1-(2-Aminophenyl)pyrroles and Benzoquinones/Ketones

A metal-free trifluorosulfonate anhydride (TFAA)-catalyzed strategy for the synthesis of spiro pyrrolo[1,2-a]quinoxalines from 1-(2-aminophenyl)pyrroles and benzoquinones/ketones has been developed. With this general method, spiro pyrrolo[1,2-a]quinoxalin

Copper-catalyzed tandem aerobic oxidative cyclization for the synthesis of 4-cyanoalkylpyrrolo[1,2-a]quinoxalines from 1-(2-aminophenyl)pyrroles and cyclobutanone oxime esters

A copper-catalyzed tandem ring-opening/cyclization reaction for the synthesis of 4-cyanoalkylpyrrolo[1,2-a]quinoxalines from 1-(2-aminophenyl)pyrroles and cyclobutanone oxime esters has been developed. This reaction involves C-C bond cleavage and C-C and C-N bond constructions with good functional group tolerance. A wide range of products are obtained in moderate to good yields under mild conditions.

FeCl3-Catalyzed synthesis of pyrrolo[1,2-: A] quinoxaline derivatives from 1-(2-aminophenyl)pyrroles through annulation and cleavage of cyclic ethers

A straightforward Fe-catalyzed method for the synthesis of pyrrolo[1,2-a]quinoxalines from 1-(2-aminophenyl)pyrroles and cyclic ethers, which includes functionalization of C(sp3)-H bonds and the construction of C-C and C-N bonds, has been devel