70787-31-4

Basic information

• Product Name: 2-(2-bromophenoxy)aniline
• Synonyms: 2-(2-bromophenoxy)aniline
• CAS NO: 70787-31-4
• Molecular Formula: C₁₂H₁₀BrNO
• Molecular Weight: 264.1179
• Mol File: 70787-31-4.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-bromophenoxy)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-bromophenoxy)aniline(70787-31-4)
• EPA Substance Registry System: 2-(2-bromophenoxy)aniline(70787-31-4)

Safety Data

• Hazardous Substances Data: 70787-31-4(Hazardous Substances Data)

Usage

Chemical structure

Consists of a benzene ring with a bromine atom and an aniline group attached.

Usage

Commonly used in the synthesis of pharmaceuticals, dyes, and other organic compounds.

Functionality

Presence of the bromine atom and aniline group makes it useful for various chemical reactions and functional group transformations.

Biological activity

Can be used as a starting material for the preparation of biologically active molecules and has been studied for its potential applications in medicinal chemistry and drug discovery.

Synthesis intermediate

Demonstrated potential as an intermediate in the synthesis of various organic compounds, making it a valuable tool for chemical research and development.

Upstream product

• 95-56-7 2-hydroxybromobenzene 
• 1493-27-2 ortho-nitrofluorobenzene 
• 88-73-3 2-Chloronitrobenzene 
• 2216-12-8 1-nitro-2-phenoxy-benzene 
• 60671-89-8 1-(2-bromophenoxy)-2-nitrobenzene 
• 56966-62-2 1-(2-nitrophenoxy)-4-bromobenzene 

Downstream Products

• 958244-59-2 2-bromo-1-(2-iodophenoxy)benzene 
• 958244-60-5 (2-(2-bromophenoxy)phenyl)diphenylphosphine 
• 1225-16-7 10-phenyl-10H-phenoxaphosphinine 
• 204847-21-2 N-(2-(2-bromophenoxy)phenyl)acetamide 
• 51452-87-0 2,2'-dibromodiphenyl ether 
• 135-67-1 phenoxazine 
• 6192-43-4 1-(10H-phenoxazin-10-yl)ethan-1-one 
• 1403815-63-3 C₃₀H₂₀BrN₃O₃ 
• 1403815-62-2 C₃₀H₂₃BrN₂O₃ 
• 1316274-10-8 (+)-(S)-4-bromo-10-benzoyl-11-methyl-10,11-dihydrodibenzo[b,f][1,4]oxazepine 
• 1091-27-6 10-phenyl-10λ⁵-phenoxaphosphine 10-oxide 

Relevant articles and documents

Microwave assisted rapid synthesis of phenoxazines and benzopyridoxazines

A facile protocol for the synthesis of phenoxazines and benzopyridoxazines by Smiles rearrangement have been demonstrated in short reaction time under microwave irradiation. The control experiments suggest that a reaction proceeds through Smiles rearrangement followed SNAr ring closure by in situ cascade process. In our present work, both the electron donating and electron withdrawing groups were tolerant and provided a corresponding phenoxazine/benzopyridoxazine in good to moderate yields.

Pyrazinamide compounds, preparation method and application thereof as well as bactericide

The invention relates to the field of pesticide bactericides and discloses pyrazinamide compounds, a preparation method and an application thereof as well as a bactericide. The compounds have the structure shown in formula (I). The pyrazinamide compounds with the novel structure are designed by introducing pyrazine ring fragments in Pyradiflumid and diphenyl ether fragments with wide bioactivity,and the pyrazinamide compounds can be used as novel SDHIs (succinate dehydrogenase inhibitors) or bactericides.

An efficient domino Sonogashira/double carbopalladation/C-H-activation reaction leading to fluorescent polycyclic aromatic hydrocarbons

A facile synthesis of fluorescent polycyclic aromatic hydrocarbons through a highly productive palladium-catalyzed fourfold domino Sonogashira/double carbopalladation/C-H-activation process was developed.