5044-39-3

Basic information

• Product Name: 1-(4-BROMO-PHENYL)-1H-PYRROLE
• Synonyms: 1-(4-BROMO-PHENYL)-1H-PYRROLE;1-(4-BROMOPHENYL)PYRROLE
• CAS NO: 5044-39-3
• Molecular Formula: C₁₀H₈BrN
• Molecular Weight: 222.08
• Product Categories: pharmacetical
• Mol File: 5044-39-3.mol
• Article Data: 41

Chemical Properties

• Melting Point: 91-92 °C
• Boiling Point: 283°C at 760 mmHg
• Flash Point: 124.9°C
• Appearance: /
• Density: 1.38g/cm³
• Vapor Pressure: 0.00556mmHg at 25°C
• Refractive Index: 1.605
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: -5.87±0.70(Predicted)
• CAS DataBase Reference: 1-(4-BROMO-PHENYL)-1H-PYRROLE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-BROMO-PHENYL)-1H-PYRROLE(5044-39-3)
• EPA Substance Registry System: 1-(4-BROMO-PHENYL)-1H-PYRROLE(5044-39-3)

Safety Data

• HazardClass: IRRITANT
• Hazardous Substances Data: 5044-39-3(Hazardous Substances Data)

Usage

General Description

1-(4-Bromo-phenyl)-1H-pyrrole is a type of organic compound that belongs to the pyrrole and phenyl groups. This chemical is often characterized by its molecular structure which contains a bromine atom attached to the fourth carbon atom in the phenylethene chain and a pyrrole ring. Pyrroles are heterocyclic aromatic organic compounds, made of five atoms including one nitrogen atom. The presence of the bromine can make it useful for various chemical reactions and industrial applications, as bromine compounds are typically used as intermediates in organic synthesis. Its properties such as molecular weight, boiling point, solubility, and toxicity would be determined through scientific analysis. Overall, as a chemical compound, 1-(4-Bromo-phenyl)-1H-pyrrole is mostly used in research and industrial processes.

InChI:InChI=1/C10H8BrN/c11-9-3-5-10(6-4-9)12-7-1-2-8-12/h1-8H

Upstream product

• 696-59-3 cis,trans-2,5-dimethoxytetrahydrofuran 
• 106-40-1 4-bromo-aniline 
• 109-97-7 pyrrole 
• 589-87-7 1,4-bromoiodobenzene 
• 106-49-0 p-toluidine 
• 62-53-3 aniline 
• 586-78-7 para-nitrophenyl bromide 
• 30438-95-0 N,N-diallyl-4-bromobenzenamine 
• 6117-80-2 1,4-butenediol 
• 860361-86-0 1-(4-bromo-phenyl)-2,5-dihydro-pyrrole 

Downstream Products

• 74986-21-3 dimethyl 1-(4-bromophenyl)pyrrole-3,4-dicarboxylate 
• 74986-14-4 dimethyl (E)-1-(4-bromophenyl)-2-pyrrolyl-2-butenedioate 
• 74986-02-0 dimethyl (Z)-1-(4-bromophenyl)-2-pyrrolyl-2-butenedioate 
• 22106-33-8 4-(1H-pyrrole-1-yl)benzoic acid 
• 354115-80-3 1-(4-Bromo-3-carboxyphenyl)pyrrole 
• 133662-27-8 5-bromo-2-(1H-pyrrol-1-yl)benzoic acid 
• 445399-41-7 C₁₀H₇Br₃NP 
• 23351-05-5 1-(4’-formylphenyl)pyrrole 
• 916667-70-4 1-(4-(N-tert-butyl-N-hydroxylamino)phenyl)pyrrole 
• 445399-46-2 C₁₈H₂₃BrN₃O₂PS 
• 445399-54-2 C₁₈H₂₂Br₃N₃O₂P₂S 
• 959706-68-4 2-[4-(1H-pyrrol-1-yl)phenyl]hexanal 
• 1004111-79-8 5-(4-(1H-pyrrol-1-yl)phenyl)furan-2-carbaldehyde 
• 477849-05-1 C₁₂H₇BrCl₃NO 

Relevant articles and documents

New Pyrrole-Based Organic Dyes for Dye-Sensitized Solar Cells: Convenient Syntheses and High Efficiency

Harvesting the sunshine : Two new pyrrole-containing organic dyes were rationally designed and easily prepared. Thanks to the special electronic properties of pyrrole moieties and the introduction of the non-coplanar aromatic rings through a single bond (

A solvent-free manganese(II) -catalyzed Clauson-Kaas protocol for the synthesis of N-aryl pyrroles under microwave irradiation

The first manganese-catalyzed modified Clauson-Kaas reaction for N-substituted pyrrole synthesis using 2,5-dimethoxytetrahydrofuran with variously substituted aromatic amines has been developed (up to 89% yield). This interesting neat strategy is free from additives including co-catalysts, ligands, and acids. Relatively low cost, environmentally benign, and handy Mn(NO3)2·4H2O is employed as the catalyst under microwave conditions with a very short reaction time (20?min). The above qualities attest to the green nature of this reaction.

A facile synthesis of 1-aryl pyrroles by clauson-Kaas reaction using oxone as a catalyst under microwave irradiation

A new and efficient methodology to synthesize N-substituted pyrrole derivatives by Clauson Kaas reaction employing Oxone as catalyst was developed. The transformation was performed in acetonitrile under microwave irradiation. This procedure has several advantages such as high yield, clean product formation, and short reaction time.

MICROCAPSULES AND PROCESSES FOR THEIR PREPARATION

The present invention provides microcapsules encapsulating hydrophilic or hydrophobic active agents in an inorganic shell, processes for their preparation and compositions comprising them.