2,6-DIFLUORO-3-METHOXYBENZAMIDE

95%

Reagent Code: #176883
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CAS Number 886498-26-6

science Other reagents with same CAS 886498-26-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.1500 g/mol
Formula C₈H₇F₂NO₂
badge Registry Numbers
MDL Number MFCD04115900
thermostat Physical Properties
Boiling Point 214.1±40.0 °C
inventory_2 Storage & Handling
Density 1.331±0.06 g/cm3
Storage 2-8°C, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its fluorinated aromatic structure, which enhances metabolic stability and binding affinity in drug molecules. Also employed in the preparation of bioactive agents targeting inflammatory and neurological disorders. Its amide and methoxy functionalities allow for further chemical modifications, making it valuable in structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿17,440.00
inventory 10mg
10-20 days ฿32,650.00

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2,6-DIFLUORO-3-METHOXYBENZAMIDE
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its fluorinated aromatic structure, which enhances metabolic stability and binding affinity in drug molecules. Also employed in the preparation of bioactive agents targeting inflammatory and neurological disorders. Its amide and methoxy functionalities allow for further chemical modifications, making it

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its fluorinated aromatic structure, which enhances metabolic stability and binding affinity in drug molecules. Also employed in the preparation of bioactive agents targeting inflammatory and neurological disorders. Its amide and methoxy functionalities allow for further chemical modifications, making it valuable in structure-activity relationship studies.

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