5-TRIFLUOROMETHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID

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Reagent Code: #48463
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CAS Number 869782-94-5

science Other reagents with same CAS 869782-94-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.14 g/mol
Formula C₉H₅F₃N₂O₃
badge Registry Numbers
MDL Number MFCD06739135
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethoxy group and an indazole core, makes it valuable in the design of potential drug candidates, particularly those targeting enzyme inhibition or receptor modulation. Researchers often explore its derivatives for applications in treating conditions such as inflammation, cancer, and neurological disorders. Additionally, its chemical properties are leveraged in medicinal chemistry to enhance the pharmacokinetic and pharmacodynamic profiles of experimental compounds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,022.00
inventory 1g
10-20 days ฿28,224.00
inventory 50mg
10-20 days ฿4,644.00

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5-TRIFLUOROMETHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID
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This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethoxy group and an indazole core, makes it valuable in the design of potential drug candidates, particularly those targeting enzyme inhibition or receptor modulation. Researchers often explore its derivatives for applications in treating conditions such as inflammation, can

This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethoxy group and an indazole core, makes it valuable in the design of potential drug candidates, particularly those targeting enzyme inhibition or receptor modulation. Researchers often explore its derivatives for applications in treating conditions such as inflammation, cancer, and neurological disorders. Additionally, its chemical properties are leveraged in medicinal chemistry to enhance the pharmacokinetic and pharmacodynamic profiles of experimental compounds.

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