N-Cyclopropyl 4-fluorobenzamide

98%

Reagent Code: #219503
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CAS Number 88229-16-7

science Other reagents with same CAS 88229-16-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.19 g/mol
Formula C₁₀H₁₀FNO
badge Registry Numbers
MDL Number MFCD03363521
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows activity in modulating biological pathways involved in cell proliferation. Employed in research settings to design potent and selective drug candidates targeting specific enzymes. Also utilized in agrochemical research for developing new active ingredients with improved metabolic stability. Its structural features enhance binding affinity and bioavailability in lead optimization stages.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,120.00
inventory 25g
10-20 days ฿3,990.00
inventory 100g
10-20 days ฿13,890.00

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N-Cyclopropyl 4-fluorobenzamide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows activity in modulating biological pathways involved in cell proliferation. Employed in research settings to design potent and selective drug candidates targeting specific enzymes. Also utilized in agrochemical research for developing new active ingredients with improved metabolic stability. Its structural features enhance binding affinity and bioavailabili

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Shows activity in modulating biological pathways involved in cell proliferation. Employed in research settings to design potent and selective drug candidates targeting specific enzymes. Also utilized in agrochemical research for developing new active ingredients with improved metabolic stability. Its structural features enhance binding affinity and bioavailability in lead optimization stages.

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