13979-81-2

Usage

Uses

Used in Laboratory Research:
3,5-DIBROMO-4-METHYLPHENOL is used as a research chemical for [application reason] in laboratory settings. Its unique properties allow for its use in various experimental procedures and studies.
Used in Industrial Applications:
3,5-DIBROMO-4-METHYLPHENOL is used as an industrial chemical for [application reason] in the manufacturing process. Its functional groups contribute to its role in the production of various products.
Used in Synthesis of Polymers:
3,5-DIBROMO-4-METHYLPHENOL is used as a starting material for the synthesis of polymers. Its chemical structure provides a foundation for the creation of new polymer compounds with specific properties.
Used in Pharmaceutical Industry:
3,5-DIBROMO-4-METHYLPHENOL is used as a starting material in the synthesis of pharmaceuticals. Its presence in the molecular structure of certain drugs can contribute to their therapeutic effects.
Used in Dye Industry:
3,5-DIBROMO-4-METHYLPHENOL is used as a starting material in the production of dyes. Its chemical properties allow for the creation of dyes with unique color characteristics.
Safety Precautions:
Despite its wide range of applications, 3,5-DIBROMO-4-METHYLPHENOL can be hazardous to health if accidentally ingested or inhaled. Therefore, it is crucial to exercise caution during its handling and follow proper safety protocols to minimize risks.

InChI:InChI=1/C7H6Br2O/c1-4-6(8)2-5(10)3-7(4)9/h2-3,10H,1H3

Upstream product

• 2432-14-6 3,5-dibromo-4-hydroxytoluene 
• 13194-73-5 3,5-dibromo-4-methylaniline 
• 344249-21-4 2,5-dibromo-p-cresol 
• 37721-75-8 tetrabromo-p-cresol 
• 106-44-5 p-cresol 
• 7446-70-0 aluminium trichloride 
• 6627-55-0 2-bromo-p-cresol 
• 71-43-2 benzene 
• 39953-10-1 2,4,6-tribromo-4-methylcyclohexa-2,5-dienone 
• 36776-51-9 2,3,6-tribromo-4-methyl-phenol 
• 77339-24-3 2,3,4,6-tetrabromo-4-methylcyclohexa-2,5-dienone 

Downstream Products

• 151101-40-5 2,3,5-tribromo-4-methyl-phenol 
• 37721-75-8 tetrabromo-p-cresol 
• 861343-81-9 2,3,6-tribromo-4-methoxy-toluene 
• 871339-63-8 O-(3,5-dibromo-4-methylphenyl)dimethylthiocarbamate 
• 871340-27-1 C₂₈H₄₄N₄O₂ 
• 871340-28-2 C₂₈H₄₈N₄O₂ 
• 871464-92-5 C₁₉H₃₂N₄O 
• 871464-82-3 C₂₁H₃₆N₄O 
• 871465-04-2 C₂₃H₄₀N₄ 
• 871340-25-9 C₂₂H₃₆N₄O₃ 
• 871341-72-9 C₂₆H₃₇BrN₈O 
• 871340-24-8 C₁₆H₂₃BrN₂O₃ 
• 1407499-93-7 C₃₀H₄₇Br₂NO₇Si₂ 
• 1407499-94-8 (4,6-dibromo-2-((4,5-dimethoxy-2-nitrobenzyl)oxy)-5-methyl-1,3-phenylene)dimethanol 

Relevant academic research and scientific papers

Electrophilic Substitution with Rearrangement. Part 9. Dienones derived from Brominations of o-, m-, and p-Cresol

Regiospecific protodebromination of ring-substituted bromophenols derived from 2-, 3-, or 4-methylphenol can be effected by heating them with aqueous hydrogen iodide; the synthetic scope of this reaction has been explored.These di- and poly-bromophenols can generally be converted by further bromination in aqueous acetic acid into dienones , which have now been shown to have the 4-bromo-2,5-dienone rather than the 2-bromo-3,5-dienone structure.The rearrangemens of these dienones to ring-substituted polybromophenols by treatment with sulfuric acid have been investigated; where more than one product is formed, the regioselectivity differs from that prevailing in the corresponding direct bromination of the phenol with liquid bromine.The alternative rearrangements of these dienones in aprotic solvents with and without illumination have been compared with results obtained by reaction of methylphenols with bromine under the same conditions.Characteristic differences between the behaviours of 2-, 3-, and 4-methyl-substituted compounds reflect the specific reactions available to the particular dienones.