104147-32-2

Basic information

• Product Name: 3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline
• Synonyms: 3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline;3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)benzenamine
• CAS NO: 104147-32-2
• Molecular Formula: C₈H₅Cl₂F₄NO
• Molecular Weight: 278.03
• EINECS: 401-790-3
• Product Categories: Intermediate
• Mol File: 104147-32-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 305 °C
• Flash Point: 138 °C
• Appearance: Kind of white to yellow powder
• Density: 1.558
• Vapor Pressure: 0.000834mmHg at 25°C
• Refractive Index: 1.496
• Storage Temp.: 2-8°C
• PKA: 1.82±0.10(Predicted)
• CAS DataBase Reference: 3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline(104147-32-2)
• EPA Substance Registry System: 3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline(104147-32-2)

Safety Data

• Hazard Codes: Xn,N
• Statements: 22-50/53
• Safety Statements: 24/25-26-57-60-61
• Hazardous Substances Data: 104147-32-2(Hazardous Substances Data)

Usage

General Description

3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline is a chemical compound with the molecular formula C8H6Cl2F4NO. It is a synthetic compound that contains both chlorine and fluorine atoms, making it a halogenated organic compound. It is commonly used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other industrial chemicals. 3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline is also known for its potential use as a pesticide and herbicide due to its ability to inhibit the growth of certain plants and pests. As with all chemical compounds, proper handling and disposal of 3,5-Dichloro-4-(1,1,2,2-tetrafluoroethoxy)aniline is necessary to minimize environmental and health risks.

InChI:InChI=1/C8H5Cl2F4NO/c9-4-1-3(15)2-5(10)6(4)16-8(13,14)7(11)12/h1-2,7H,15H2

Upstream product

• 87-65-0 2,6-Dichlorophenol 
• 116-14-3 polytetrafluoroethylene 
• 5930-28-9 4-amino-2,6-dichlorophenol 

Downstream Products

• 104147-33-3 3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenylisocyanate 
• 1415750-46-7 2-((6-chloropyridin-3-yl)methoxy)-N-(3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl)benzamide 
• 1261132-07-3 N-[2-(cyclohexylamino)-1-(3-fluorophenyl)-2-oxoethyl]-N-[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]-4-methyl-1,2,3-thiadiazole-5-carboxamide 
• 1261132-04-0 N-[2-(cyclohexylamino)-2-oxo-1-m-tolylethyl]-N-(3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl)-4-methyl-1,2,3-thiadiazole-5-carboxamide 
• 1261132-13-1 N-[2-(cyclohexylamino)-1-(2-methoxyphenyl)-2-oxoethyl]-N-[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]-4-methyl-1,2,3-thiadiazole-5-carboxamide 
• 1261132-14-2 N-[2-(cyclohexylamino)-1-(3-methoxyphenyl)-2-oxoethyl]-N-[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]-4-methyl-1,2,3-thiadiazole-5-carboxamide 
• 1261132-06-2 N-[2-(cyclohexylamino)-1-(2-fluorophenyl)-2-oxoethyl]-N-[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]-4-methyl-1,2,3-thiadiazole-5-carboxamide 
• 1261132-12-0 N-[2-(cyclohexylamino)-1-(3-hydroxyphenyl)-2-oxoethyl]-N-[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]-4-methyl-1,2,3-thiadiazole-5-carboxamide 
• 1261131-99-0 N-[1-(3-chlorophenyl)-2-(cyclohexylamino)-2-oxoethyl]-N-[3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)phenyl]-4-methyl-1,2,3-thiadiazole-5-carboxamide 

Relevant articles and documents

Production technology of 3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)benzenamine

The invention discloses a production technology of 3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)benzenamine, and relates to the technical field of chemical product production. 2,6-dichlorophenol and nitric acid are mixed to be subjected to a nitration reaction, and 2,6-dichloro-4-nitrophenol (DCNP) is obtained; the 2,6-dichloro-4-nitrophenol (DCNP) is subjected to a reduction reaction in hydrogen, and 4-amino-2,6-dichlorophenol (DCAP) is obtained; then, the 4-amino-2,6-dichlorophenol (DCAP) and tetrafluoroethylene are subjected to an addition reaction, and 3,5-dichloro-4-(1,1,2,2-tetrafluoroethoxy)benzenamine is obtained. The reaction purpose is strong, few by-products are produced, the conversion rate is high, and postprocessing is easy.