657-02-3

Basic information

• Product Name: 3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE
• Synonyms: 3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE;3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE, 97% MIN.;2,3-Dichloro-5-(trifluoromethyl)nitrobenzene;1,2-Dichloro-3-nitro-5-(trifluoroMethyl)benzene;4,5-Dichloro-3-nitrobenzotrifluoride
• CAS NO: 657-02-3
• Molecular Formula: C₇H₂Cl₂F₃NO₂
• Molecular Weight: 260
• Mol File: 657-02-3.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 239.3±35.0℃ (760 Torr)
• Flash Point: 98.6±25.9℃
• Appearance: /
• Density: 1.638±0.06 g/cm3 (20 ºC 760 Torr)
• Vapor Pressure: 0.0623mmHg at 25°C
• Refractive Index: 1.511
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE(657-02-3)
• EPA Substance Registry System: 3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE(657-02-3)

Safety Data

• Hazard Codes: Xi
• Statements: 20/21/22
• Safety Statements: 36/37/39-45
• HazardClass: IRRITANT, IRRITANT-HARMFUL
• Hazardous Substances Data: 657-02-3(Hazardous Substances Data)

Usage

Description

3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE is an organic compound characterized by the presence of two chlorine atoms at the 3rd and 4th positions, a nitro group at the 5th position, and three fluorine atoms attached to the benzene ring. 3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE is known for its chemical reactivity and is commonly used as an intermediate in the synthesis of various organic compounds.

Uses

Used in Pharmaceutical Industry:
3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE is used as a chemical intermediate for the preparation of 2,6-Dichloro-4-trifluoromethylphenylamine, which is an important compound in the synthesis of certain pharmaceuticals. The unique structure of 3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE allows for the formation of specific chemical bonds that are crucial for the development of these pharmaceuticals.
Used in Chemical Synthesis:
3,4-DICHLORO-5-NITROBENZOTRIFLUORIDE is used as a reagent in various chemical reactions, such as substitution, addition, and elimination reactions. Its presence of electron-withdrawing groups makes it a versatile compound for the synthesis of a wide range of organic compounds, including dyes, agrochemicals, and other specialty chemicals.

InChI:InChI=1/C7H2Cl2F3NO2/c8-4-1-3(7(10,11)12)2-5(6(4)9)13(14)15/h1-2H

Upstream product

• 328-84-7 1,2-dichloro-4-(trifluoromethyl)benzene 

Downstream Products

• 50594-32-6 1-Chloro-3-nitro-2-phenoxy-5-trifluoromethyl-benzene 
• 101646-02-0 5-Chloro-4-fluoro-3-nitro-trifluoromethylbenzene 
• 57729-79-0 2-chloro-6-nitro-4-(trifluoromethyl)aniline 
• 69741-64-6 2-chloro-6-nitro-4-(trifluoromethyl)phenol 
• 1647-76-3 7-chloro-2-methyl-1-phenyl-5-trifluoromethyl-1H-benzoimidazole 
• 789-82-2 3-chloro-N²-phenyl-5-trifluoromethyl-o-phenylenediamine 
• 50594-81-5 5-amino-3,4-dichloro-α,α,α-trifluorotoluene 
• 2709-95-7 (2-chloro-6-nitro-4-trifluoromethyl-phenyl)-phenyl-amine 
• 50594-33-7 3-Chloro-2-phenoxy-5-trifluoromethyl-phenylamine 
• 50594-34-8 2,6-Dichlor-4-trifluormethyl-diphenylether 
• 42874-36-2 1,3-Dichloro-2-(4-nitro-phenoxy)-5-trifluoromethyl-benzene 

Relevant articles and documents

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The herbicidal-4-trifluoromethyl-3'-carbon-substituted-4'-substituted diphenyl ethers comprise a class of compounds that are highly effective herbicides.

Herbicidal 4-trifluoromethyl-4-nitrodiphenyl ethers

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