2-Bromo-1-(2-(difluoromethoxy)phenyl)ethanone

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Reagent Code: #124076
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CAS Number 405921-09-7

science Other reagents with same CAS 405921-09-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.05 g/mol
Formula C₉H₇BrF₂O₂
badge Registry Numbers
MDL Number MFCD01910076
inventory_2 Storage & Handling
Storage -20°C, inert gas

description Product Description

This compound is primarily utilized in the synthesis of various pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) with potential therapeutic applications. Its structure, featuring a difluoromethoxy group, makes it valuable in medicinal chemistry for designing molecules with enhanced metabolic stability and bioavailability. It is often employed in the preparation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Additionally, it serves as a key building block in organic synthesis, enabling the creation of complex molecules for drug discovery and development. Its reactive bromoacetyl group allows for further functionalization, making it a versatile reagent in chemical research.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿5,931.00
inventory 25g
10-20 days ฿19,899.00
inventory 1g
10-20 days ฿1,638.00

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2-Bromo-1-(2-(difluoromethoxy)phenyl)ethanone
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This compound is primarily utilized in the synthesis of various pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) with potential therapeutic applications. Its structure, featuring a difluoromethoxy group, makes it valuable in medicinal chemistry for designing molecules with enhanced metabolic stability and bioavailability. It is often employed in the preparation of compounds targeting specific biological pathways, such as enzyme inhibition or receptor modulation. Additionally, it serves as a key building block in organic synthesis, enabling the creation of complex molecules for drug discovery and development. Its reactive bromoacetyl group allows for further functionalization, making it a versatile reagent in chemical research.
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