960077-86-5

Basic information

• Product Name: 2-Bromo-7-phenylnaphthalene
• Synonyms: 2-Bromo-7-phenylnaphthalene
• CAS NO: 960077-86-5
• Molecular Formula: C16H11Br
• Molecular Weight: 283.16254
• Mol File: 960077-86-5.mol
• Article Data: 5

Chemical Properties

• Melting Point: 100-101℃
• Appearance: /
• CAS DataBase Reference: 2-Bromo-7-phenylnaphthalene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Bromo-7-phenylnaphthalene(960077-86-5)
• EPA Substance Registry System: 2-Bromo-7-phenylnaphthalene(960077-86-5)

Safety Data

• Hazardous Substances Data: 960077-86-5(Hazardous Substances Data)

Usage

Description

2-Bromo-7-phenylnaphthalene is a chemical compound that features a naphthalene ring with a bromine atom at the 2-position and a phenyl group connected to the 7-position. 2-Bromo-7-phenylnaphthalene is known for its role as a reagent in organic synthesis, particularly for the production of pharmaceuticals and agrochemicals.

Uses

Used in Pharmaceutical Industry:
2-Bromo-7-phenylnaphthalene is used as a reagent for the synthesis of various pharmaceuticals, contributing to the development of new drugs and improving existing ones.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-7-phenylnaphthalene is utilized as a reagent in the synthesis of agrochemicals, which are essential for enhancing crop protection and productivity.
Used in Organic Synthesis:
2-Bromo-7-phenylnaphthalene serves as a building block in the synthesis of a wide range of organic compounds, playing a crucial role in advancing the field of chemistry.
It is important to handle 2-Bromo-7-phenylnaphthalene with care due to its toxic nature, which can cause skin and eye irritation upon contact. Proper safety measures and environmental regulations should be followed for its storage and disposal.

Upstream product

• 58556-75-5 2,7-dibromonaphthalene 
• 98-80-6 phenylboronic acid 
• 591-50-4 iodobenzene 
• 1337916-21-8 7-bromonaphthalen-2-ylboronic acid 

Relevant articles and documents

COMPOUND FOR ORGANIC OPTOELECTRONIC DEVICE, COMPOSITION FOR ORGANIC OPTOELECTRONIC DEVICE, ORGANIC OPTOELECTRONIC DEVICE AND DISPLAY DEVICE

The invention relates to a compound for an organic optoelectronic device, a composition for an organic optoelectronic device, an organic optoelectronic device and a display device. A compound for an organic optoelectronic device, a composition for an orga

1-(α-Aminobenzyl)-2-naphthol as phosphine-free ligand for Pd-catalyzed Suzuki and one-pot Wittig-Suzuki reaction

Air stable and easily accessible, 1-(α-aminobenzyl)-2-naphthols are used as efficient phosphine-free ligands in palladium-catalyzed Suzuki reaction for a variety of substrates under conventional heating as well as ultrasonic conditions. Multi-brominated aromatic substrates were successfully converted to corresponding arylated moieties with good conversion and selectivity. A novel one-pot two-step cascade reaction strategy involving Wittig and Suzuki reactions is developed for efficient synthesis of 4-styryl biphenyls (C 6-C2-C6-C6 unit). Copyright 2012 John Wiley & Sons, Ltd. Phosphine free 1-(α-aminobenzyl)-2- naphthol ligands are used for Pd catalyzed Suzuki and one-pot Wittig-Suzuki reaction to efficiently prepare styryl biphenyls (C6-C 2-C6-C6 unit). Copyright

Synthesis of C-aryl-nucleosides and O-aryl-glycosides via cuprate glycosylation

(Chemical Equation Presented) 2′-Deoxy-C-aryl-nucleosides have found increasing importance in studying DNA-DNA and DNA-protein interactions, as unnatural DNA-base pairs, and as oligonucleotide based fluorophores. Access to the required C-aryl-nucleosides