3-(Boc-amino)-6-fluoro-1H-indazole

≥95%

Reagent Code: #69466
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CAS Number 1176089-41-0

science Other reagents with same CAS 1176089-41-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.26 g/mol
Formula C₁₂H₁₄FN₃O₂
badge Registry Numbers
MDL Number MFCD18651681
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of various indazole-based compounds, which are known for their potential therapeutic applications. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective manipulation of the amine functionality during synthetic processes, enabling the construction of complex molecular structures. Additionally, the fluorine substituent enhances the compound's ability to interact with biological targets, making it valuable in the design of drug candidates targeting specific enzymes or receptors. Its application is particularly relevant in the development of treatments for diseases such as cancer, inflammation, and neurological disorders, where indazole derivatives have shown promising activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿10,620.00
inventory 5g
10-20 days ฿23,004.00

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3-(Boc-amino)-6-fluoro-1H-indazole
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of various indazole-based compounds, which are known for their potential therapeutic applications. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective manipulation of the amine functionality during synthetic processes, enabling the construction of complex molecular struct

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of biologically active molecules. It serves as a key intermediate in the creation of various indazole-based compounds, which are known for their potential therapeutic applications. The presence of the Boc (tert-butoxycarbonyl) protecting group allows for selective manipulation of the amine functionality during synthetic processes, enabling the construction of complex molecular structures. Additionally, the fluorine substituent enhances the compound's ability to interact with biological targets, making it valuable in the design of drug candidates targeting specific enzymes or receptors. Its application is particularly relevant in the development of treatments for diseases such as cancer, inflammation, and neurological disorders, where indazole derivatives have shown promising activity.

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