Ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate

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Reagent Code: #184728
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CAS Number 885271-93-2

science Other reagents with same CAS 885271-93-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 222.22 g/mol
Formula C₁₁H₁₁FN₂O₂
badge Registry Numbers
MDL Number MFCD06739128
thermostat Physical Properties
Boiling Point 366.9±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.317±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key 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 the presence of the indazole core, which is known for its biological activity. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) targeting tyrosine kinases and other signaling enzymes involved in tumor growth. Also utilized in research settings for structure-activity relationship (SAR) studies to optimize drug candidates. Its ester functionality allows for easy modification, enabling the introduction of various side chains to enhance potency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,000.00
inventory 250mg
10-20 days ฿8,770.00
inventory 1g
10-20 days ฿16,140.00

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Ethyl 2-(5-fluoro-1H-indazol-3-yl)acetate
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Used as a key 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 the presence of the indazole core, which is known for its biological activity. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) targeting tyrosine kinases and other signaling enzymes involved in tumor growth. Also utilized in research settings for structure-activity relationship (SAR) studies to optimize drug candidates. Its ester functionality allows for easy modification, enabling the introduction of various side chains to enhance potency and selectivity.
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