14505-17-0

Basic information

• Product Name: Benzene, 1-nitro-4-(tribromomethyl)-
• CAS NO: 14505-17-0
• Molecular Formula: C7H4Br3NO2
• Molecular Weight: 373.826
• Mol File: 14505-17-0.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1-nitro-4-(tribromomethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-nitro-4-(tribromomethyl)-(14505-17-0)
• EPA Substance Registry System: Benzene, 1-nitro-4-(tribromomethyl)-(14505-17-0)

Safety Data

• Hazardous Substances Data: 14505-17-0(Hazardous Substances Data)

Usage

General Description

Benzene, 1-nitro-4-(tribromomethyl)- is a chemical compound with the molecular formula C6H4Br3NO2. It is a nitro-substituted compound with a tribromomethyl group attached to the benzene ring. This chemical is commonly used in the production of agricultural chemicals, pharmaceuticals, and dyes. It is classified as a hazardous substance due to its toxic and carcinogenic properties, and exposure to this chemical can cause harmful effects on the central nervous system, liver, and kidneys. Therefore, it is important to handle and store this chemical with care and follow proper safety protocols when using it in industrial or research settings.

Upstream product

• 619-75-0 1-dibromomethyl-4-nitro-benzene 
• 402-54-0 p-nitrobenzotrifluoride 
• 99-99-0 1-methyl-4-nitrobenzene 
• 127-09-3 sodium acetate 

Downstream Products

• 402-54-0 p-nitrobenzotrifluoride 
• 7553-56-2 iodine 
• 132586-45-9 4-hydroxybenzoic acid 4'-trifluoromethylphenyl ester 
• 35852-57-4 2,6-dibromo-4-(trifluoromethyl)phenol 
• 3337-62-0 3,5-dibromo-4-hydroxybenzoic acid 
• 349-97-3 4-(trifluromethyl)acetanilide 
• 402-43-7 p-trifluoromethylphenyl bromide 
• 455-13-0 4-Iodobenzotrifluoride 
• 402-45-9 4-hydroxybenzotrifluoride 
• 339-42-4 N-((4-trifluoromethyl)phenyl)-4-aminobenzene sulphonamide 
• 455-14-1 4-trifluoromethylphenylamine 
• 94781-50-7 α-deuterio-4-nitro-benzaldehyde 
• 73908-63-1 <1-²H₂>-p-nitrobenzyl alcohol 
• 83327-12-2 p-nitro(α,α-D2)benzyl chloride 

Relevant articles and documents

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Catalytic halodefluorination of aliphatic carbon-fluorine bonds

A variety of halosilanes, in conjunction with aluminum catalysts, convert fluorocarbons into higher halocarbons. Bromination and iodination of fluorocarbons are more effective than chlorination in terms of yield and activity. The mechanism for the reaction is investigated utilizing experimental and computational evidence and preliminary results suggest an alternate mechanism to that reported for the related hydrodefluorination reaction.

Benzylic Bromination-Acetoxylation of Toluenes by Bromide Ion Catalyzed Thermal Decomposition of Peroxydisulfate in Acetic Acid in the Presence of Acetate Ions

Side-chain bromination and acetoxylation of alkylaromatics by halide ion induced decomposition of potassium peroxydisulfate in acetic acid have been studied by product analysis techniques.Catalytic amounts of lithium bromide in the presence of sodium acetate were found effective in promoting benzylic bromination, followed by conversion to the corresponding benzyl acetates by reaction with acetate.The reaction is interpreted to take place by the redox and free-radical chain mechanism involving bromine atoms (ρ = -1.38 vs. ? + for substituted toluenes).In competiti ve experiments, benzyl and 4-nitrobenzyl acetates were found lees reactive than the corresponding toluenes in acetic acid with the couple S2O82-/Br- but more reactive in carbon tetrachloride with N-bromosuccinimide.