4-Bromo-1-(difluoromethoxy)-2-methylbenzene

97%

Reagent Code: #120098
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CAS Number 888327-32-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.04 g/mol
Formula C₈H₇BrF₂O
badge Registry Numbers
MDL Number MFCD11036069
thermostat Physical Properties
Boiling Point 223°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active compounds. Its unique structure, featuring a difluoromethoxy group, makes it valuable in the development of molecules with enhanced biological activity and metabolic stability. In pharmaceuticals, it is often employed in the creation of drugs targeting specific receptors or enzymes, particularly in the fields of oncology and neurology. In agrochemicals, it serves as a building block for the production of pesticides and herbicides, contributing to improved efficacy and selectivity. Additionally, its bromine atom allows for further functionalization, enabling the creation of diverse derivatives for research and industrial applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 10g
10-20 days $112.07
inventory 250mg
10-20 days $16.23
inventory 1g
10-20 days $16.62
inventory 5g
10-20 days $58.74
4-Bromo-1-(difluoromethoxy)-2-methylbenzene
This chemical is primarily utilized in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of various active compounds. Its unique structure, featuring a difluoromethoxy group, makes it valuable in the development of molecules with enhanced biological activity and metabolic stability. In pharmaceuticals, it is often employed in the creation of drugs targeting specific receptors or enzymes, particularly in the fields of oncology and neurology. In agrochemicals, it serves as a building block for the production of pesticides and herbicides, contributing to improved efficacy and selectivity. Additionally, its bromine atom allows for further functionalization, enabling the creation of diverse derivatives for research and industrial applications.
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