45859-98-1

Usage

Uses

Used in Pharmaceutical Synthesis:
2,4,6-Tribromobenzaldehyde is used as a key intermediate in the production of pharmaceuticals, contributing to the development of new drugs and medicines. Its chemical structure allows for further reactions and modifications that can lead to the creation of a wide range of therapeutic compounds.
Used in Agrochemical Production:
In the agrochemical industry, 2,4,6-Tribromobenzaldehyde is employed as a starting material for the synthesis of various agrochemicals, such as pesticides and herbicides. Its presence in these compounds can enhance their effectiveness in controlling pests and weeds, thereby supporting agricultural productivity.
Used in Organic Compound Synthesis:
2,4,6-Tribromobenzaldehyde is utilized as a building block in the synthesis of a variety of organic compounds, including dyes, polymers, and other specialty chemicals. Its reactivity and structural features make it a valuable component in the creation of complex molecules with specific properties.
Used as a Flame Retardant in Polymer and Plastic Manufacturing:
2,4,6-Tribromobenzaldehyde is incorporated into the production of polymers and plastics as a flame retardant. Its chemical composition helps to inhibit the ignition and spread of fires, making it a crucial component in the development of safer materials for various applications.
Used in Laboratory Research:
2,4,6-Tribromobenzaldehyde is employed as a reagent in laboratory settings for the derivatization of various organic compounds. Its ability to react with a range of substances makes it a useful tool in chemical research and analysis.
Safety Precautions:
It is important to handle 2,4,6-Tribromobenzaldehyde with care due to its corrosive nature and potential to cause irritation to the skin, eyes, and respiratory system. Proper safety measures, such as wearing protective gear and working in a well-ventilated area, should be taken to minimize risks associated with its use.

Upstream product

• 626-39-1 1,3,5-trisbromobenzene 
• 68-12-2 N,N-dimethyl-formamide 
• 633-12-5 2,4,6-tribromobenzoic acid 
• 54459-64-2 2,4,6-tribromo-1-(bromomethyl)benzene 
• 107-06-2 1,2-dichloro-ethane 
• 71642-16-5 3-methyl-2,4,6-tribromoaniline 
• 1709-44-0 m-aminobenzaldehyde 
• 22019-73-4 2,4,6-Tribrombenzylalkohol 
• 861605-41-6 3-amino-2,4,6-tribromo-benzaldehyde 
• 6320-40-7 2,4,6-tribromotoluene 

Downstream Products

• 763110-62-9 (2,4,6-tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)methanol 
• 2537-67-9 2,4,6-tribromoacetophenone 
• 714293-45-5 [2,4,6-tris(trimethylsilylethynyl)phenyl](4-tert-butyl-2,6-dimethylphenyl)diazomethane 
• 714293-50-2 C₃₄H₄₆Si₃ 
• 714293-44-4 [2,4-bis(trimethylsilylethynyl)-6-bromophenyl](4-tert-butyl-2,6-dimethylphenyl)diazomethane 
• 714293-49-9 C₂₉H₃₇BrSi₂ 
• 714293-48-8 (4-trimethylsilyl-2,6-dibromophenyl)(4-tert-butyl-2,6-dimethylphenyl)carbene 
• 763110-74-3 (3,5-bis-{3,5-dibromo-4-[(4-tert-butyl-2,6-dimethyl-phenyl)-diazo-methyl]-phenylethynyl}-phenylethynyl)-trimethyl-silane 
• 763110-72-1 (4-tert-butyl-2,6-dimethyl-phenyl)-(2,6-dibromo-4-{3-[3,5-dibromo-4-(4-tert-butyl-2,6-dimethyl-benzoyl)-phenylethynyl]-5-trimethylsilanylethynyl-phenylethynyl}-phenyl)-methanone 
• 763110-68-5 (4-tert-butyl-2,6-dimetgylphenyl)[2,6-dibromo-4-(trimethylsilylethynyl)phenyl]methanone 
• 763110-69-6 (4-tert-butyl-2,6-dimethylphenyl)(2,6-dibromo-4-ethynylphenyl)methanone 
• 763110-67-4 (2,6-dibromo-4-ethynylphenyl)-(2,6-dimethyl-4-tert-butylphenyl)diazomethane 
• 714293-43-3 (4-trimethylsilylethynyl-2,6-dibromophenyl)(4-tert-butyl-2,6-dimethylphenyl)diazomethane 
• 848075-08-1 ethyl N-nitroso-N-[(2,4,6-tribromophenyl)(4-tert-butyl-2,6-dimethylphenyl)methyl]carbamate 

Relevant academic research and scientific papers

Regiospecific metalation of oligobromobenzenes

The metalation of selected oligobromobenzenes with lithium diisopropylamide (LDA) was investigated. 1,3-Dibromo-substituted benzenes were metalated without special precautions since the resultant 2,6-dibromophenyllithium intermediates are relatively stabl

Synthesis of 1,3,6,8-tetrabromophenanthrene via a stoichiometric Ullmann reaction

1,3,6,8-Tetrabromophenantherene (1) is prepared in four steps from 2,4,6-tribromobenzoic acid (4) in an overall yield of 12%. The key transformation used in the synthesis is a stoichiomteric Ullmann reaction.

Method of preparing substituted benzaldehydes

A process for the preparation of Benzaldehydes substituted in the nucleus is disclosed by oxidation of the corresponding benzyl halides. The process is performed in the presence of water using aminoxides of tertiary amines.