5-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carboxylic acid

≥95%

Reagent Code: #86793
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CAS Number 850893-02-6

science Other reagents with same CAS 850893-02-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.16 g/mol
Formula C₁₃H₁₃BrN₂O₃
badge Registry Numbers
MDL Number MFCD30489523
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of indazole derivatives. These derivatives are often explored for their potential therapeutic applications, such as enzyme inhibition or receptor modulation. The tetrahydro-2H-pyran-2-yl group in the structure enhances its stability and reactivity, making it suitable for further chemical modifications. Researchers also employ it in the design of drug candidates targeting specific diseases, including cancer and inflammatory disorders, due to its unique structural features.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,980.00

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5-Bromo-1-(tetrahydro-2H-pyran-2-yl)-1H-indazole-3-carboxylic acid
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This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of indazole derivatives. These derivatives are often explored for their potential therapeutic applications, such as enzyme inhibition or receptor modulation. The tetrahydro-2H-pyran-2-yl group in the structure enhances its stability and reactivity, making it suitable for further chemical modificatio

This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active molecules, particularly in the synthesis of indazole derivatives. These derivatives are often explored for their potential therapeutic applications, such as enzyme inhibition or receptor modulation. The tetrahydro-2H-pyran-2-yl group in the structure enhances its stability and reactivity, making it suitable for further chemical modifications. Researchers also employ it in the design of drug candidates targeting specific diseases, including cancer and inflammatory disorders, due to its unique structural features.

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