4995-11-3

Basic information

• Product Name: 1H-Pyrrole, 2-(4-bromophenyl)-
• CAS NO: 4995-11-3
• Molecular Formula: C10H8BrN
• Molecular Weight: 222.084
• Mol File: 4995-11-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrole, 2-(4-bromophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrole, 2-(4-bromophenyl)-(4995-11-3)
• EPA Substance Registry System: 1H-Pyrrole, 2-(4-bromophenyl)-(4995-11-3)

Safety Data

• Hazardous Substances Data: 4995-11-3(Hazardous Substances Data)

Usage

Structure

A derivative of pyrrole, a five-membered aromatic heterocycle with a nitrogen atom, with a bromine atom attached to the 2-position of the pyrrole ring and a phenyl group with a bromine atom at the 4-position attached to the pyrrole ring.

Usage

In organic synthesis and medicinal chemistry as a building block for the synthesis of various biologically active compounds.

Potential applications

In material science, as a starting material for the production of polymers and functional materials.

Upstream product

• 59862-55-4 p-bromoacetophenone oxime 
• 74-86-2 acetylene 
• 109-97-7 pyrrole 
• 5467-74-3 4-Bromophenylboronic acid 
• 65826-67-7 bis(4-bromophenyl)iodonium bromide 
• 1616603-25-8 C₁₂H₁₂BrNO₂ 
• 1122-91-4 4-bromo-benzaldehyde 
• 106650-98-0 1-(4-bromophenyl)but-3-en-1-ol 
• 184165-64-8 1-(4-bromophenyl)-3-buten-1-one 
• 1607800-84-9 tert-butyl 2-(4-bromophenyl)-1H-pyrrole-1-carboxylate 
• 589-87-7 1,4-bromoiodobenzene 
• 673-40-5 4-bromobenzenediazonium tetrafluoroborate 

Downstream Products

• 91735-78-3 2-(4-bromophenyl)-5-trifluoroacetylpyrrole 
• 1623807-55-5 N-(2-(2-(4-bromophenyl)-1H-pyrrol-1-yl)ethyl)-4-methyl-N-((1-tosyl-1H-1,2,3-triazol-4-yl)methyl)benzenesulfonamide 
• 1623807-67-9 N-((7-(4-bromophenyl)-3-tosyl-2,3,4,5-tetrahydro-1H-pyrrolo[1,2-d][1,4]diazepin-1-yl)methyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Fabrication of Graphitic Carbon Nitride-Based Film: An Emerged Highly Efficient Catalyst for Direct C—H Arylation under Solar Light

Photoredox C—H bond formation can proceed in aerobic environment under solar light and has therefore become attractive. Nowadays, different types of expensive novel metal complexes and nanomaterials have been urbanized as photocatalysts for direct C—H bon

Copper-catalyzed 5-endo-trig cyclization of ketoxime carboxylates: A facile synthesis of 2-arylpyrroles

A novel and facile copper-catalyzed 5-endo-trig cyclization of ketoxime carboxylates for the synthesis of 2-arylpyrroles has been developed. The reaction tolerates a range of functional groups and is a practical procedure for rapid synthesis of 2-arylpyrroles in high yields under mild conditions. the Partner Organisations 2014.

Iron-mediated direct suzuki-miyaura reaction: A new method for the ortho -arylation of pyrrole and pyridine

(Figure presented) The first example of an iron-mediated direct Suzuki-Miyaura reaction between N-heterocyclic compounds and arylboronic acids is described, and both electron-rich and electron-deficient heteroarenes can be successfully used for the coupling reaction.