2-(2,6-Difluorophenyl)-N-methoxy-N-methylacetamide

≥95%

Reagent Code: #177279
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CAS Number 946402-24-0

science Other reagents with same CAS 946402-24-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.20 g/mol
Formula C₁₀H₁₁F₂NO₂
badge Registry Numbers
MDL Number MFCD24809494
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Widely used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its structure allows for efficient introduction of the difluorophenyl moiety, which enhances metabolic stability and binding affinity in drug molecules. Commonly employed in medicinal chemistry for constructing complex bioactive compounds, especially in the design of kinase inhibitors and CNS-targeted therapeutics. The methoxy methyl amide group facilitates coupling reactions and serves as a masked carboxylic acid equivalent in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,920.00
inventory 250mg
10-20 days ฿27,360.00

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2-(2,6-Difluorophenyl)-N-methoxy-N-methylacetamide
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Widely used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its structure allows for efficient introduction of the difluorophenyl moiety, which enhances metabolic stability and binding affinity in drug molecules. Commonly employed in medicinal chemistry for constructing complex bioactive compounds, especially in the design of kinase inhibitors and CNS-targeted therapeutics. The methoxy methyl amide group f

Widely used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its structure allows for efficient introduction of the difluorophenyl moiety, which enhances metabolic stability and binding affinity in drug molecules. Commonly employed in medicinal chemistry for constructing complex bioactive compounds, especially in the design of kinase inhibitors and CNS-targeted therapeutics. The methoxy methyl amide group facilitates coupling reactions and serves as a masked carboxylic acid equivalent in multi-step syntheses.

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