1203578-65-7

Basic information

• Product Name: 2-Phenyl-7-BroMoquinoline
• Synonyms: 2-Phenyl-7-BroMoquinoline;7-broMo-2-phenylquinoline
• CAS NO: 1203578-65-7
• Molecular Formula: C₁₅H₁₀BrN
• Molecular Weight: 284.1506
• Mol File: 1203578-65-7.mol
• Article Data: 19

Chemical Properties

• Melting Point: 122.0-123.5℃
• Appearance: /
• Density: 1.433±0.06 g/cm3 (20℃ 760 Torr)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2-Phenyl-7-BroMoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenyl-7-BroMoquinoline(1203578-65-7)
• EPA Substance Registry System: 2-Phenyl-7-BroMoquinoline(1203578-65-7)

Safety Data

• Hazardous Substances Data: 1203578-65-7(Hazardous Substances Data)

Usage

General Description

2-Phenyl-7-Bromoquinoline is a chemical compound with the molecular formula C16H10BrN. It is a member of the quinoline family and is characterized by a phenyl group attached to the 2-position and a bromine atom attached to the 7-position of the quinoline ring. 2-Phenyl-7-BroMoquinoline is used in various research and industrial applications, including as a building block for the synthesis of pharmaceuticals and agrochemicals. It has also been studied for its potential biological activities, such as antimicrobial and anticancer properties. 2-Phenyl-7-Bromoquinoline may also be used as a fluorescent dye or as a reagent in organic synthesis.

Upstream product

• 59278-65-8 2-amino-4-bromobenzaldehyde 
• 98-86-2 acetophenone 
• 946122-05-0 (2-amino-4-bromophenyl)methanol 
• 98-85-1 1-Phenylethanol 
• 115976-33-5 1-phenyl (O,1-⁽²⁾H₂)ethanol 
• 98-80-6 phenylboronic acid 
• 860720-24-7 7-bromoquinoline 1-oxide 
• 5551-12-2 4-bromo-2-nitrobenzaldehyde 
• 1636-34-6 2,3-diphenyl-2,3-butanediol 
• 19433-17-1 acetophenone O-acetyloxime 
• 4965-36-0 7-bromoquinoline 
• 100-59-4 phenylmagnesium chloride 

Downstream Products

• 1253106-87-4 1,1-diphenyl-N-((2-phenylquinolin-7-yl)methylene)methanamine 
• 408508-52-1 7-amino-2-phenylquinoline 
• 27356-39-4 7-methyl-2-phenylquinoline 

Relevant articles and documents

Visible-Light-Induced Amination of Quinoline at the C8 Position via a Postcoordinated Interligand-Coupling Strategy under Mild Conditions

The postcoordinated interligand-coupling strategy provides a useful and complementary protocol for synthesizing polydentate ligands. Herein, diastereoselective photoreactions of Λ-[Ir(pq)2(d-AA)] (Λ-d) and Λ-[Ir(pq)2(l-AA)] (Λ-l, where pq is 2-phenylquino

Mild and efficient copper-catalyzed oxidative cyclization of oximes with 2-aminobenzyl alcohols at room temperature: synthesis of polysubstituted quinolines

A simple and efficient ligand-free Cu-catalyzed protocol for the synthesis of polysubstituted quinolinesviaoxidative cyclization of oxime acetates with 2-aminobenzyl alcohols at room temperature has been developed. The presented approach provides a new synthetic pathway leading to polysubstituted quinolines with good functional group tolerance under mild conditions. Moreover, this transformation can be applied for the preparation of quinolines on a gram scale. Oxime acetates serve as the internal oxidants in the reactions, thus making this method very attractive.

Ruthenium-catalyzed acceptorless dehydrogenative coupling of o-aminobenzyl alcohols with ketones to quinolines in the presence of carbonate salt

A ruthenium complex bearing a functional 2,2′-bibenzimidazole ligand [(p-cymene)Ru(BiBzImH2)Cl][Cl] was designed, synthesized and found to be a general and highly efficient catalyst for the synthesis of quinolines via acceptorless dehydrogenative coupling of o-aminobenzyl alcohols with ketones in the presence of carbonate salt. It was confirmed that NH units in the ligand are crucial for catalytic activity. The application of this catalytic system for the scale-gram synthesis of biologically active molecular was also undertaken. Notably, this research exhibits new potential of metal–ligand bifuctional catalysts for acceptorless dehydrogenative reactions.