133152-04-2

Usage

Uses

Used in Organic Chemistry:
2,6-Dichloro-4-trifluoromethylphenylazide is utilized as a reagent in organic chemistry for the synthesis of azide-derived molecules. Its reactivity allows for the formation of a variety of complex organic structures that are valuable in numerous applications.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2,6-Dichloro-4-trifluoromethylphenylazide is used as a key intermediate in the development of new drugs. Its unique structure and reactivity contribute to the creation of novel pharmaceutical compounds with potential therapeutic benefits.
Used in Material Science:
2,6-Dichloro-4-trifluoromethylphenylazide also finds use in the development of new materials, where its properties can be harnessed to produce materials with specific characteristics required for various applications.
Used in Photochemistry and Photophysics:
Due to its photochemical properties, 2,6-Dichloro-4-trifluoromethylphenylazide has potential applications in the field of photochemistry and photophysics. It can be involved in reactions that are triggered or influenced by light, opening up possibilities for its use in light-sensitive materials and processes.
Despite the inherent risks associated with its explosive nature, 2,6-Dichloro-4-trifluoromethylphenylazide holds substantial value in the field of chemical research and development, driving innovation in synthesis and material science.

Upstream product

• 24279-39-8 2,6-dichloro-4-(trifluoromethyl)aniline 

Downstream Products

• 133152-01-9 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-methylsulphonyl-1 H-1,2,3-triazole 
• 133177-43-2 1-(2,6-dichloro-4-trifluoromethylphenyl)-4-nitro-1 H-1,2,3-triazole 
• 1096363-07-3 [1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-[1,2,3]triazol-4-ylmethyl]diethylamine 
• 1096363-09-5 4-(1-cyclohexenyl)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-[1,2,3]triazole 
• 1096363-14-2 4-(benzyloxymethyl)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-[1,2,3]triazole 
• 1096363-11-9 1-[1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-[1,2,3]triazol-4-yl]-cyclohexanol 
• 1096363-16-4 4-(bromomethyl)-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-[1,2,3]triazole 
• 1096363-05-1 2-[1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-1H-[1,2,3]triazol-4-yl]propan-2-ol 
• 1610967-74-2 C₉H₄Cl₂F₃N₃ 
• 1610967-91-3 C₁₃H₈F₃N₉ 
• 1610967-84-4 C₉H₃Cl₂F₃N₄O₂ 

Relevant academic research and scientific papers

Synthesis, 3D-QSAR, and docking studies of 1-phenyl-1H-1,2,3-triazoles as selective antagonists for β3 over α1β2γ2 GABA receptors

A series of 16 1-phenyl-1H-1,2,3-triazoles with substituents at both the 4- and 5-positions of the triazole ring were synthesized, and a total of 49 compounds, including previously reported 4- or 5-monosubstituted analogues, were examined for their abilit

Regioselective synthesis of 1-(2,6-dichloro-4-trifluoromethylphenyl)-4- alkyl-1H-[1,2,3]-triazoles

A new and efficient method for the synthesis of 1-(2,6-dichloro-4- trifluoromethylphenyl)-4-alkyl-1H-[1,2,3]-triazoles by the room temperature 1,3-dipolar cycloaddition of (2-azido-1,3-dichloro-5-trifluoromethyl)benzene with terminal alkynes in the presen

Synthesis and structure-activity relationships of 1-phenyl-1H-1,2,3- triazoles as selective insect GABA receptor antagonists

To study the interaction of phenylheterocycles with γ-aminobutyric acid (GABA) receptors, 4- or 5-alkyl-(or phenyl)-1-phenyl-1H-1,2,3-triazoles were synthesized and examined for their ability to inhibit the specific binding of [3H]-4′-ethynyl-4

2-imidazol(in)e substituted aryl-1,2,3-triazole pesticides

Compounds of formula I STR1 and salts thereof, in which Ar, W, Z, A, R1-7, Y, m, p and n have the meanings given in the description, have pesticidal activity especially against insects, acarids and animal endoparasites.

Triazole pesticides

Compounds of formula I in which Ar is phenyl, pyridyl or pyrimidinyl, each of which is optionally substituted, and X and Z, which may be the same or different, are as defined in the description, have insecticidal and acaricidal activity. Many compounds ar