85598-12-5

Usage

Uses

Used in Pharmaceutical Industry:
4-Bromo-3-methyl-2-nitrophenol is used as a chemical intermediate for the synthesis of pharmaceuticals, contributing to the development of new drugs due to its reactive functional groups.
Used in Agricultural Chemicals:
In the agricultural sector, 4-Bromo-3-methyl-2-nitrophenol is utilized as an intermediate in the production of agricultural chemicals, potentially enhancing crop protection and yield.
Used in Dye and Pigment Manufacturing:
4-Bromo-3-methyl-2-nitrophenol is employed as a key component in the manufacturing of dyes and pigments, providing a range of color options for various applications.
Used in Antibacterial Research:
4-Bromo-3-methyl-2-nitrophenol is used in research as a potential antibacterial agent, being studied for its ability to combat bacterial infections and contribute to the development of new antibiotics.
Safety Considerations:
It is important to handle 4-Bromo-3-methyl-2-nitrophenol with care due to its toxic nature if ingested or inhaled, and its potential to cause skin and eye irritation. Proper safety measures should be implemented during its use and disposal to minimize health risks.

Upstream product

• 14472-14-1 4-bromo-3-methylphenol 
• 50-85-1 2-hydroxy-p-toluic acid 
• 108-39-4 3-methyl-phenol 
• 6623-35-4 5-bromo-2-hydroxy-4-methylbenzoic acid 
• 64-19-7 acetic acid 

Downstream Products

• 85598-13-6 1-bromo-4-methoxy-2-methyl-3-nitro-benzene 
• 1154740-49-4 5-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine 
• 1154740-48-3 6-bromo-5-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazine 
• 1154740-46-1 2-amino-4-bromo-3-methylphenol 
• 786596-55-2 2-Methyl-3-bromo-6-methoxyaniline 
• 85598-20-5 1-(p-Toluenesulfonyl)-4-methoxy-4-indoleacetonitrile 
• 85598-17-0 N-(p-Toluenesulfonyl)-4-formyl-7-methoxyindole 
• 85598-18-1 N-(p-Toluenesulfonyl)-4-hydroxymethyl-7-methoxyindole 
• 85598-19-2 N-(p-Toluenesulfonyl)-4-chloromethyl-7-methoxyindole 
• 85628-22-4 N,N-Dimethyl-2-(2-nitro-3-methoxy-6-cyanophenyl)ethenamine 
• 85598-14-7 2-Nitro-3-methyl-4-cyanoanisole 
• 436093-34-4 (2R,3S)-3-[7-Methoxy-1-(toluene-4-sulfonyl)-1H-indol-4-yl]-1-trityloxy-butan-2-ol 
• 436091-70-2 3-[1-(tert-butyl-dimethyl-silanyl)-7-methoxy-1H-indol-4-yl]-1-trityloxy-butan-2-ol 
• 436091-30-4 N-(5-{1-[7-methoxy-1-(toluene-4-sulfonyl)-1H-indol-4-yl]-ethyl}-1H-imidazol-2-yl)-acetamide 

Relevant academic research and scientific papers

Enantioselective synthesis of the aminoimidazole segment of dragmacidin D

A facile enantioselective synthesis of the 2-aminoimidazole side-chain of dragmacidin D has been developed, which involved the regio- and stereoselective opening of the chiral epoxide 9 by a diindolylcuprate reagent, followed by further steps to give 5-substituted N-(1H-imidazol-2-yl)acetamide 2.