2-Bromo-5-fluoro-4-methylaniline
≥95%
Reagent
Code: #116727
CAS Number
202865-78-9
blur_circular Chemical Specifications
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Molecular Information
Weight
204.04 g/mol
Formula
C₇H₇BrFN
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Registry Numbers
MDL Number
MFCD00142871
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Physical Properties
Boiling Point
245.3°C at 760 mmHg
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Storage & Handling
Storage
Room temperature, away from light, stored in an inert gas
description Product Description
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex compounds. Its structure, featuring bromo, fluoro, and methyl substituents on an aniline ring, makes it a versatile building block for creating molecules with potential biological activity. In pharmaceuticals, it is often employed in the development of drugs targeting specific receptors or enzymes, particularly in the design of small-molecule inhibitors or modulators. In agrochemicals, it serves as a precursor for the production of herbicides, fungicides, or insecticides, where its unique substitution pattern can enhance the efficacy and selectivity of the final product. Additionally, it is used in organic research for the development of novel chemical entities, leveraging its reactivity in coupling reactions, halogen exchange processes, or functional group transformations.
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2-Bromo-5-fluoro-4-methylaniline
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex compounds. Its structure, featuring bromo, fluoro, and methyl substituents on an aniline ring, makes it a versatile building block for creating molecules with potential biological activity. In pharmaceuticals, it is often employed in the development of drugs targeting specific receptors or enzymes, particularly in the design of small-molecule inhibitors or modulators. In agrochemicals, it serves as a precursor for the production of herbicides, fungicides, or insecticides, where its unique substitution pattern can enhance the efficacy and selectivity of the final product. Additionally, it is used in organic research for the development of novel chemical entities, leveraging its reactivity in coupling reactions, halogen exchange processes, or functional group transformations.
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