4-bromo-N-methyl-2-nitroaniline

97%

Reagent Code: #218268
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CAS Number 53484-26-7

science Other reagents with same CAS 53484-26-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.0467 g/mol
Formula C₇H₇BrN₂O₂
badge Registry Numbers
MDL Number MFCD00624242
thermostat Physical Properties
Melting Point 97.5-98 °C
Boiling Point 316.1 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.687 g/cm3
Storage 2-8°C, away from light, dry

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and dyes. Its structure allows for further functionalization in organic reactions, making it valuable in creating complex aromatic compounds. Commonly employed in Sandmeyer and coupling reactions to introduce bromine and nitro groups into larger molecules. Also utilized in research settings for the preparation of substituted anilines and heterocyclic compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿720.00
1g
10-20 days ฿1,530.00
5g
10-20 days ฿5,240.00
25g
10-20 days ฿22,010.00
10g
10-20 days ฿10,440.00
4-bromo-N-methyl-2-nitroaniline
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and dyes. Its structure allows for further functionalization in organic reactions, making it valuable in creating complex aromatic compounds. Commonly employed in Sandmeyer and coupling reactions to introduce bromine and nitro groups into larger molecules. Also utilized in research settings for the preparation of substituted anilines and heterocyclic compounds.

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and dyes. Its structure allows for further functionalization in organic reactions, making it valuable in creating complex aromatic compounds. Commonly employed in Sandmeyer and coupling reactions to introduce bromine and nitro groups into larger molecules. Also utilized in research settings for the preparation of substituted anilines and heterocyclic compounds.

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