273735-64-1

Basic information

• Product Name: 2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline
• Synonyms: 2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline
• CAS NO: 273735-64-1
• Molecular Weight: 330.032
• Mol File: 273735-64-1.mol

Chemical Properties

• CAS DataBase Reference: 2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline(273735-64-1)
• EPA Substance Registry System: 2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline(273735-64-1)

Safety Data

• Hazardous Substances Data: 273735-64-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drug molecules.
Used in Agrochemical Industry:
In the agrochemical sector, 2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline is utilized as a building block in the creation of agrochemicals, potentially enhancing the effectiveness of pesticides and other agricultural products.
Used in Dye Industry:
2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline is employed in the dye industry as an intermediate, contributing to the production of various dyes with specific color properties and stability.
Used in Specialty Chemicals Synthesis:
2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline is used as a key component in the synthesis of specialty chemicals, which may have applications in various fields such as coatings, adhesives, and plastics.
Used in Research Applications:
In the field of research, this compound serves as a valuable tool for scientists, aiding in the exploration of new chemical reactions and the development of novel chemical entities.
Used in Material Science:
2,6-dichloro-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]aniline has potential applications in material science, where it may be used to develop new materials with unique properties, such as improved thermal stability or chemical resistance.
It is important to handle this compound with care, as it may pose health and environmental risks if not properly managed.

Upstream product

• 62-53-3 aniline 
• 2396-17-0 4-perfluoroisopropylaniline 

Downstream Products

• 1126745-48-9 3-amino-4-bromo-N-[2,6-dichloro-4-(1,2,2,2-tetrafluoro-1-trifluoromethylethyl)phenyl]benzamide 
• 1267507-99-2 N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-nitrobenzamide 
• 1267508-04-2 4-amino-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide 
• 1267508-06-4 4-amino-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide 
• 1267507-48-1 3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-iodobenzamide 
• 1267507-92-5 3-chloro-4-cyano-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide 
• 1267506-56-8 tert-butyl (2-chloro-4-{[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]carbamoyl}benzyl)carbamate 
• 1267506-31-9 4-(aminomethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide 
• 1267506-32-0 4-(acetamidemethyl)-3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]benzamide 
• 1267506-33-1 3-chloro-N-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]-4-[(propionylamino)methyl]benzamide 
• 1401000-55-2 4-[2,6-dichloro-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenylcarbamoyl]-naphthalene-1-carboxylic acid methyl ester 
• 1334128-68-5 2-azido-1,3-dichloro-5-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]benzene 
• 1416900-81-6 methyl 2-chloro-5-{1-[2,6-dichloro-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)phenyl]1H-1,2,3-triazol-4-yl}benzoate 
• 1416900-80-5 2-chloro-5-{1-[2,6-dichloro-4-(1,2,2,2-tetrafluoro-1-trifluoromethyl-ethyl)-phenyl]-1H-[1,2,3]triazol-4-yl}-benzoic acid 

Relevant articles and documents

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The present invention provides an aniline derivative represented by the formula (I) wherein R1 and R2 are each H, (C1-12)alkyl, (C3-8)cycloalkyl, hydroxy(C1-12)alkyl, hydroxycarbonyl (C1-12)alkyl, (C1-6)-alkoxycarbonyl(C1-6)alkyl, —COR8, wherein R8 is H, halo-(C1-12)alkyl, (C3-8)cycloalkyl or (substituted) phenyl, COOR9, wherein R9 is a halo(C1-6)alkyl group, (substituted) phenyl or (substituted) benzyl; R3, R4, R5, R6and R7 are each H, halogen, OH, nitro, halo(C1-12)alkylthio, (substituted)amino-(C1-2)alkyl, (substituted) phenyl, (substituted) benzyl, amino, —N(R10)R11 wherein R10 and R11 are each H, alkyl, cycloalkyl, (substituted) phenyl, (substituted) benzyl, —COR8 or COOR9, or (C2-27)perfluoroalkyl, etc., and a process for producing the aniline derivative. According to the process of the present invention, perfluoroalkylaniline derivatives can be obtained by using various anilines as the substrate with a high position selectivity and high yield.