1682-04-8

Usage

Uses

Used in Pharmaceutical and Agrochemical Industries:
4-Bromo-2,3,5,6-tetrafluoroanisole is used as an intermediate in the synthesis of pharmaceuticals and agrochemicals for its ability to contribute to the development of new drugs and pesticides.
Used in Organic Chemistry:
In the field of organic chemistry, 4-Bromo-2,3,5,6-tetrafluoroanisole is utilized as a building block for the preparation of various organic compounds, highlighting its role in creating complex organic molecules.
Used in Specialty Chemicals Production:
4-Bromo-2,3,5,6-tetrafluoroanisole is an important reagent for the production of specialty chemicals, which are used across a wide range of industrial applications due to their unique properties.
Used in Advanced Materials Development:
4-BroMo-2,3,5,6-tetrafluoroanisole also plays a role in the development of advanced materials, contributing to innovations in various industries that require high-performance materials.

Upstream product

• 344-04-7 bromopentafluorobenzene 
• 124-41-4 sodium methylate 
• 67-56-1 methanol 

Downstream Products

• 32777-48-3 3-(p-Methoxytetrafluorphenyl)propen 
• 2324-98-3 2,3,5,6-tetrafluoroanisole 
• 33068-38-1 2-Brom-1-(p-methoxytetrafluorphenyl)-propan 
• 32777-49-4 2-Azido-1-(p-methoxytetrafluorophenyl)-propan 
• 46495-46-9 2-(p-Methoxy-tetrafluorphenyl)-1-methyl-aethylamin 
• 1149763-62-1 tetrakis(2,3,5,6-tetrafluoro-4-methoxyphenyl) lithium borate 
• 77896-34-5 2,4'-dimethoxy-2',3',5',6'-tetrafluorobenzophenone 
• 77896-23-2 2,4'-dihydroxy-2',3',5',6'-tetrafluorobenzophenone 
• 77896-33-4 (2-methoxyphenyl)-4-methoxy-2,3,5,6-tetrafluorophenylmethanol 

Relevant academic research and scientific papers

Regiospecific Syn Addition of (Polyfluoroaryl)copper Reagents to Fluorinated Acetylenes: Preparation and Subsequent Functionalization of Internal Vinylcopper Reagents

(Pentafluorophenyl)copper (C6F5Cu) can be prepared from a metathesis reaction between C6F5CdX (X = Br or C6F5) and CuY (Y = Cl or Br).The arylcopper reagent undergoes a stereo- and regiospecific syn addition to fluorinated alkynes, which results in the corresponding internal alkenylcopper intermediate.This vinylcopper reagent can be subsequently functionalized with a variety of electrophiles, including aryl, alkyl, allyl, and acyl halides, to afford tetrasubstituted fluoroalkenes.The para-substituted arylcopper analogs also successfully undergo the addition reaction.

Synthesis and Herbicidal Activity of Phenylproparginols

A three-step/one-pot procedure was developed for preparing herbicidal fluorophenylproparginols from acetophenones by way of an enol phosphate intermediate.Side-by-side testing of 16 of the more active analogs showed that trans-2-methyl-1-2-(4-methoxy-2,3