911836-38-9

Basic information

• Product Name: 1-Bromo-5-phenylnaphthalene
• Synonyms: 1-Bromo-5-phenylnaphthalene
• CAS NO: 911836-38-9
• Molecular Formula: C₁₆H₁₁Br
• Molecular Weight: 283.16254
• Mol File: 911836-38-9.mol

Chemical Properties

• Boiling Point: 385.8±11.0 °C(Predicted)
• Appearance: /
• Density: 1.381±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1-Bromo-5-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Bromo-5-phenylnaphthalene(911836-38-9)
• EPA Substance Registry System: 1-Bromo-5-phenylnaphthalene(911836-38-9)

Safety Data

• Hazardous Substances Data: 911836-38-9(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
1-bromo-5-phenylnaphthalene is used as a reactant in various organic synthesis reactions, contributing to the formation of new compounds with diverse applications.
Used in Electronic Materials:
1-bromo-5-phenylnaphthalene is being studied for its potential use in electronic materials due to its unique properties, which could contribute to the development of advanced electronic devices.
Used in Fluorescent Materials:
1-bromo-5-phenylnaphthalene is also being explored for its potential use in fluorescent materials, where it could be utilized in applications such as sensors, imaging, or other technologies that require fluorescence.
Safety Precautions:
It is important to handle 1-bromo-5-phenylnaphthalene with caution, as it is considered hazardous if ingested, inhaled, or absorbed through the skin. Safety precautions should be followed when working with 1-bromo-5-phenylnaphthalene, including the use of appropriate personal protective equipment and working in a well-ventilated area.

Upstream product

• 86-57-7 1-Nitronaphthalene 
• 7351-74-8 1,5-dibromonaphthalene 
• 98-80-6 phenylboronic acid 
• 4766-33-0 5-amino-1-bromonaphthalene 
• 5328-76-7 1-bromo-5-nitronaphthalene 
• 68449-30-9 5-bromo-1-tetralone 
• 911836-37-8 5-bromo-1-phenyl-1,2,3,4-tetrahydro-naphthalen-1-ol 

Downstream Products

• 76980-73-9 7-phenyl-1H-phenalen-1-one 
• 911836-29-8 1'-deoxy-1'-β-(5-phenylnaphth-1-yl)-3',5'-bis-O-tert-butyldimethylsilyl-2'-O-thionocarbonylimidazolyl-arabinose 
• 911836-33-4 1',2'-dideoxy-1'-β-(5-phenylnaphth-1-yl)-3',5'-bis-O-tert-butyldimethylsilyl-ribose 
• 911836-25-4 1'-deoxy-1'-β-(5-phenylnaphth-1-yl)-3',5'-bis-O-tert-butyldimethylsilyl-arabinose 

Relevant articles and documents

ORGANIC ELECTROLUMINESCENT ELEMENT AND MONOAMINE COMPOUND FOR ORGANIC ELECTROLUMINESCENT ELEMENT

PROBLEM TO BE SOLVED: To provide an organic electroluminescent element with high efficiency and an amine compound therefor. SOLUTION: The amine compound for organic electroluminescent element is a monoamine compound expressed by the compound, the compound

Synthesis of Positional Isomeric Phenylphenalenones

A series of isomeric phenylphenalenones in which the phenyl ring is located at all possible peripheral positions of the phenalenone nuclei was synthesized. The structural characteristics of the series, in which topological variation is permitted with minimal electronic disturbance, could, in principle, allow for easy pharmacophore recognition when the compounds are aligned in steroidomimetic conformations.

Diastereoselective synthesis of β-aryl-C-nucleosides from 1,2-anhydrosugars

(Chemical Equation Presented) The cis opening of glycal epoxides with arylaluminum reagents provides strict stereocontrol in C-glycosylation. β-Aryl-C-2-deoxynucleosides are obtained from known glycals by an epoxidation-glycosylation-deoxygenation sequenc