4-Bromo-2-chloro-N-methylaniline

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Reagent Code: #215712
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CAS Number 944131-95-7

science Other reagents with same CAS 944131-95-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.49 g/mol
Formula C₇H₇BrClN
badge Registry Numbers
MDL Number MFCD09745401
thermostat Physical Properties
Boiling Point 269.5±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.609±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block for more complex molecules due to the presence of reactive halogen groups and an aromatic amine functionality. Commonly employed in coupling reactions and nucleophilic substitutions to form carbon-nitrogen or carbon-carbon bonds. Also utilized in the development of dyes and specialty polymers where halogenated anilines enhance thermal and chemical stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,690.00
inventory 250mg
10-20 days ฿7,980.00
inventory 1g
10-20 days ฿21,500.00

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4-Bromo-2-chloro-N-methylaniline
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block for more complex molecules due to the presence of reactive halogen groups and an aromatic amine functionality. Commonly employed in coupling reactions and nucleophilic substitutions to form carbon-nitrogen or carbon-carbon bonds. Also utilized in the development of dyes and specialty polymers where halogenated anilines enhance thermal an

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the production of herbicides and fungicides. It serves as a building block for more complex molecules due to the presence of reactive halogen groups and an aromatic amine functionality. Commonly employed in coupling reactions and nucleophilic substitutions to form carbon-nitrogen or carbon-carbon bonds. Also utilized in the development of dyes and specialty polymers where halogenated anilines enhance thermal and chemical stability.

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