2,2-Difluoro-N-methoxy-N-methylacetamide

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Reagent Code: #179238
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CAS Number 142492-01-1

science Other reagents with same CAS 142492-01-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 139.10 g/mol
Formula C₄H₇F₂NO₂
badge Registry Numbers
MDL Number MFCD06248152
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Widely used in organic synthesis, this compound serves as a key reagent for the preparation of gem-difluoroalkenes, which are valuable building blocks in pharmaceutical and agrochemical development. Its structure allows for efficient difluoromethylation under mild conditions, making it particularly useful in late-stage functionalization of complex molecules. It is also employed in the synthesis of fluorinated analogs of bioactive compounds, where the presence of fluorine can enhance metabolic stability, lipophilicity, and binding affinity. Due to its stability and reactivity profile, it is favored in both academic research and industrial processes for constructing fluorinated scaffolds.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,000.00
inventory 5g
10-20 days ฿3,490.00
inventory 25g
10-20 days ฿12,810.00
inventory 100g
10-20 days ฿49,280.00

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2,2-Difluoro-N-methoxy-N-methylacetamide
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Widely used in organic synthesis, this compound serves as a key reagent for the preparation of gem-difluoroalkenes, which are valuable building blocks in pharmaceutical and agrochemical development. Its structure allows for efficient difluoromethylation under mild conditions, making it particularly useful in late-stage functionalization of complex molecules. It is also employed in the synthesis of fluorinated analogs of bioactive compounds, where the presence of fluorine can enhance metabolic stability,

Widely used in organic synthesis, this compound serves as a key reagent for the preparation of gem-difluoroalkenes, which are valuable building blocks in pharmaceutical and agrochemical development. Its structure allows for efficient difluoromethylation under mild conditions, making it particularly useful in late-stage functionalization of complex molecules. It is also employed in the synthesis of fluorinated analogs of bioactive compounds, where the presence of fluorine can enhance metabolic stability, lipophilicity, and binding affinity. Due to its stability and reactivity profile, it is favored in both academic research and industrial processes for constructing fluorinated scaffolds.

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