56966-47-3

Basic information

• Product Name: 2-(2-CHLOROPHENOXY)ANILINE
• Synonyms: 2-(2-chlorophenoxy)benzenamine
• CAS NO: 56966-47-3
• Molecular Formula: C₁₂H₁₀ClNO
• Molecular Weight: 219.67
• Mol File: 56966-47-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 304.228°C at 760 mmHg
• Flash Point: 137.792°C
• Appearance: /
• Density: 1.261g/cm³
• Vapor Pressure: 0.001mmHg at 25°C
• Refractive Index: 1.628
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-(2-CHLOROPHENOXY)ANILINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-CHLOROPHENOXY)ANILINE(56966-47-3)
• EPA Substance Registry System: 2-(2-CHLOROPHENOXY)ANILINE(56966-47-3)

Safety Data

• Hazardous Substances Data: 56966-47-3(Hazardous Substances Data)

Usage

General Description

2-(2-chlorophenoxy)aniline, also known as 2-(2-chlorophenoxy)aniline, is a chemical compound that belongs to the class of aniline derivatives. It is commonly used as an intermediate in the production of various organic compounds, including dyes, pigments, and pharmaceuticals. It is a white to light yellow solid with a slightly aromatic odor. 2-(2-CHLOROPHENOXY)ANILINE is classified as hazardous due to its potential for skin and eye irritation, as well as its toxic effects if ingested or inhaled. It is important to handle and store 2-(2-chlorophenoxy)aniline with care and to follow proper safety precautions when working with this chemical.

InChI:InChI=1/C12H10ClNO/c13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)14/h1-8H,14H2

Upstream product

• 27064-00-2 1-chloro-2-(2-nitrophenoxy)benzene 
• 1493-27-2 ortho-nitrofluorobenzene 
• 88-73-3 2-Chloronitrobenzene 
• 95-57-8 2-monochlorophenol 

Downstream Products

• 873977-74-3 N -(2-(2-chlorophenoxy)phenyl)acetamide 
• 1403815-57-5 C₃₀H₂₃ClN₂O₃ 
• 135-67-1 phenoxazine 
• 860745-37-5 acetic acid-[2-(2-chloro-4-nitro-phenoxy)-4-nitro-anilide] 
• 873386-12-0 acetic acid-[2-(2-chloro-phenoxy)-4-nitro-anilide] 
• 76840-84-1 [2-(2-Chloro-phenoxy)-phenyl]-imidazolidin-2-ylidene-amine 
• 76838-94-3 [2-(2-Chloro-phenoxy)-phenyl]-thiourea 
• 91354-11-9 1-bromo-2-(2-chlorophenoxy)benzene 

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.

DIARYL SUBSTITUTED HETEROAROMATIC COMPOUNDS

The invention relates to heterocyclic derivatives, to the use of said derivatives in treating a range of metabolic diseases and other conditions mediated by agonism of the G-protein coupled bile acid GPBAR1/TGR5 receptor, to compositions and formulations containing said derivatives, processes for their preparation and methods of delivery.