1-(tert-Butoxycarbonyl)-5-fluoro-1H-indazole-3-carboxylic acid

≥95%

Reagent Code: #86771
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CAS Number 886368-29-2

science Other reagents with same CAS 886368-29-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.25 g/mol
Formula C₁₃H₁₃FN₂O₄
badge Registry Numbers
MDL Number MFCD03840730
inventory_2 Storage & Handling
Storage -20°C, dry, sealed

description Product Description

This compound is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a fluorine substituent, makes it valuable in the design of drug candidates, particularly in the field of oncology and anti-inflammatory agents. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the indazole core. The fluorine atom enhances the metabolic stability and bioavailability of the resulting compounds, making it a useful building block in medicinal chemistry. Additionally, its carboxylic acid group provides a handle for conjugation or further chemical modifications, enabling the creation of diverse derivatives for drug discovery programs.

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inventory 250mg
10-20 days ฿28,080.00

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1-(tert-Butoxycarbonyl)-5-fluoro-1H-indazole-3-carboxylic acid
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This compound is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a fluorine substituent, makes it valuable in the design of drug candidates, particularly in the field of oncology and anti-inflammatory agents. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the indazole core. The fluori

This compound is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a fluorine substituent, makes it valuable in the design of drug candidates, particularly in the field of oncology and anti-inflammatory agents. The Boc group can be selectively removed under mild conditions, allowing for further functionalization of the indazole core. The fluorine atom enhances the metabolic stability and bioavailability of the resulting compounds, making it a useful building block in medicinal chemistry. Additionally, its carboxylic acid group provides a handle for conjugation or further chemical modifications, enabling the creation of diverse derivatives for drug discovery programs.

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