85118-24-7

Usage

Uses

Used in Organic Synthesis:
2-bromo-4-(trifluoromethyl)benzaldehyde is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for a wide range of chemical reactions, making it a valuable component in the preparation of complex organic molecules.
Used in Pharmaceutical Industry:
2-bromo-4-(trifluoromethyl)benzaldehyde is utilized as a reagent in the development of pharmaceuticals. Its presence in the molecular structure can impart specific biological activities, such as antimicrobial and anti-inflammatory properties, which are beneficial in the treatment of various diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-bromo-4-(trifluoromethyl)benzaldehyde is employed as a building block for the synthesis of agrochemicals. Its incorporation into the molecular structure of these compounds can enhance their effectiveness in controlling pests and diseases in agriculture.
Used in Fine Chemicals Industry:
2-bromo-4-(trifluoromethyl)benzaldehyde is also used in the production of fine chemicals, which are high-purity chemicals used in various applications, such as fragrances, dyes, and specialty chemicals. Its unique properties contribute to the development of novel and high-quality fine chemicals.

InChI:InChI=1/C8H4BrF3O/c9-7-3-6(8(10,11)12)2-1-5(7)4-13/h1-4H

Upstream product

• 657-64-7 2-bromo-1-(bromomethyl)-4-(trifluoromethyl)benzene 
• 68-12-2 N,N-dimethyl-formamide 
• 481075-58-5 2-bromo-1-iodo-4-(trifluoromethyl)benzene 

Downstream Products

• 1159114-81-4 (E)-1,2-di(2-bromo-4-trifluoromethyl-phenyl)ethene 
• 402-09-5 2-bromo-4-trifluoromethyl-styrene 
• 791-28-6 Triphenylphosphine oxide 
• 1131605-31-6 1-[2-bromo-4-(trifluoromethyl)phenyl]ethan-1-one 
• 349-68-8 1-(2-bromo-4-trifluoromethyl-phenyl)-ethanol 
• 954239-22-6 6-(trifluoromethyl)-1H-indazole 

Relevant academic research and scientific papers

Rationally improved chiral Bronsted acid for catalytic enantioselective allylboration of aldehydes with an expanded reagent scope

(Chemical Equation Presented) One of the most useful reactions in organic synthesis, the stereocontrolled addition of allylic metal reagents to carbonyl compounds, provides access to enantiomerically enriched homoallylic alcohols related to the acetate, propionate, and other oxygen-containing functionalities present in a large number of biologically active natural products and pharmaceutical drugs. In the search for an ideal carbonyl allylation methodology, the catalytic enantioselective allylboration presents numerous advantages such as a high chemo-, diastereo-, and enantiocontrol with stable and nontoxic pinacol allylic boronates. This article reports a rationally improved diol·SnCl4 complex as chiral protic acid catalyst, which provides unprecedented levels of enantioselectivity in the catalytic allylation, methallylation, crotylation, and 2-bromoallylation of aliphatic aldehydes. The new diol, p-F-Vivol (4b), enables a more active diol·SnCl4 catalyst that can compete more effectively with the background uncatalyzed allylboration. The usefulness of this optimized catalytic allylboration methodology was demonstrated with an efficient synthesis of the naturally occurring pyranone (+)-dodoneine and to the preparation of biologically important exomethylene-γ-lactones.

Pesticidal method using 2-phenylimidazole derivatives

The invention provides a method for the control of arthropod, plant nematode, helminth or protozoan pests using a 2-phenylimidazole derivative of the formula: STR1 wherein R1 represents hydrogen, alkyl (optionally substituted by alkoxy, alkylthio, alkylsulphinyl, alkylsulphonyl, cyano, carboxy or alkoxycarbonyl), R2 and R3, each represents hydrogen, halogen, nitro, carboxy, cyano, alkoxycarbonyl, alkanoyl, or optionally alkyl substituted carbamoyl or sulphamoyl, or amino (optionally substituted by alkyl, alkoxycarbonyl or alkanoyl) or a group R, RO, RS, RSO or RSO2 in which R represents alkyl (optionally substituted by halogen), and Ar represents a group of the formula: STR2 wherein R4 and R6 each represents halogen or a group R, RO, RS, RSO or RSO2, and R5, R7 and R8 each represents a substituent as defined for R4 and R6, or represents hydrogen, hydroxy, carboxy, nitro, cyano, amino, alkylamino (optionally substituted by alkyl, alkoxycarbonyl or alkanoyl), alkoxycarbonyl or alkanoyl or a pesticidally acceptable salt thereof, with the exclusion of compounds in which R2 and R3 simultaneously represent hydrogen atoms, compositions for use in the method and novel compounds of formula I.