tert-Butyl 3-(bromomethyl)-6-fluoro-1H-indazole-1-carboxylate

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Reagent Code: #45377
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CAS Number 174180-95-1

science Other reagents with same CAS 174180-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.1649 g/mol
Formula C₁₃H₁₄BrFN₂O₂
badge Registry Numbers
MDL Number MFCD10696846
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a bromomethyl and a fluoro group on the indazole ring, makes it a versatile building block for developing drug candidates, particularly in the field of oncology and enzyme inhibition. The tert-butyl carboxylate group provides stability and facilitates further modifications, enabling the creation of complex molecules. Researchers often employ it in medicinal chemistry to explore new therapeutic agents, focusing on its potential to interact with specific biological targets. Its role in the development of novel compounds underscores its importance in advancing drug discovery efforts.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,240.00
inventory 250mg
10-20 days ฿3,040.00

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tert-Butyl 3-(bromomethyl)-6-fluoro-1H-indazole-1-carboxylate
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This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a bromomethyl and a fluoro group on the indazole ring, makes it a versatile building block for developing drug candidates, particularly in the field of oncology and enzyme inhibition. The tert-butyl carboxylate group provides stability and facilitates further modifications, enabling the creation of complex

This compound is primarily utilized in the pharmaceutical and chemical research industries as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a bromomethyl and a fluoro group on the indazole ring, makes it a versatile building block for developing drug candidates, particularly in the field of oncology and enzyme inhibition. The tert-butyl carboxylate group provides stability and facilitates further modifications, enabling the creation of complex molecules. Researchers often employ it in medicinal chemistry to explore new therapeutic agents, focusing on its potential to interact with specific biological targets. Its role in the development of novel compounds underscores its importance in advancing drug discovery efforts.

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