38251-86-4

Basic information

• Product Name: 2-(4'-bromophenyl)-7-bromonaphthalene
• Synonyms: 2-(4'-bromophenyl)-7-bromonaphthalene
• CAS NO: 38251-86-4
• Molecular Weight: 362.063
• Mol File: 38251-86-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(4'-bromophenyl)-7-bromonaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4'-bromophenyl)-7-bromonaphthalene(38251-86-4)
• EPA Substance Registry System: 2-(4'-bromophenyl)-7-bromonaphthalene(38251-86-4)

Safety Data

• Hazardous Substances Data: 38251-86-4(Hazardous Substances Data)

Upstream product

• 38251-80-8 6-Brom-3-(4-brom-phenyl)-1-tetralol 
• 33731-92-9 3-(3-Bromo-phenyl)-2-(4-bromo-phenyl)-propionic acid 
• 38251-76-2 6-Brom-3-(4-brom-phenyl)-1-tetralon 
• 38251-75-1 3-(4-Bromphenyl)-4-(3-bromphenyl)-buttersaeure 
• 589-15-1 1-bromomethyl-4-bromobenzene 
• 830-79-5 2,4,6-trimethoxybenzaldehyde 
• 51044-13-4 4-bromobenzyl triphenylphosphonium bromide 
• 32017-76-8 (+/-)-2-(4-bromophenyl)oxirane 
• 58556-75-5 2,7-dibromonaphthalene 
• 1122-91-4 4-bromo-benzaldehyde 

Relevant articles and documents

MeOTf/KI-catalyzed efficient synthesis of 2-arylnaphthalenesviacyclodimerization of styrene oxides

The MeOTf/KI-catalyzed synthesis of 2-arylnaphthalene derivatives from aryl ethylene oxides in alcohol under ambient conditions is described. The present protocol has a higher atom efficiency and wider substrate applicability with excellent yields. The reaction proceeded using the aryl ethylene oxides to give 2-arylnaphthalenes either in homo-coupling or in cross-coupling. The reaction could also be carried out at the gram scale in minutes.

Synthesis of 2-phenylnaphthalenes from styrene oxides using a recyclable Bronsted acidic [HNMP]+HSO4- ionic liquid

This work reports a novel and efficient protocol for the synthesis of 2-phenylnaphthalenes from styrene oxides using a recyclable ionic liquid. The ionic liquid N-methyl-2-pyrrolidone hydrogensulfate [HNMP]+HSO4- played the dual role of a catalyst and a solvent. It efficiently constructs 2-phenylnaphthalene and its derivatives in excellent yields with much simplicity in the operation. The present protocol has higher atom efficiency and wider substrate applicability. The [HNMP]+HSO4- has been effectively recycled for up to five consecutive cycles without appreciable loss in its activity.

Trypanocidal diamidines with three rings in two isolated ring systems

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