5,6-DIFLUORO-1H-INDAZOLE-3-CARBOXYLIC ACID

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Reagent Code: #48011
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CAS Number 129295-33-6

science Other reagents with same CAS 129295-33-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.13 g/mol
Formula C₈H₄F₂N₂O₂
thermostat Physical Properties
Boiling Point 450.9±40.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.707±0.06 g/cm3(Predicted
Storage 2-8℃

description Product Description

5,6-Difluoro-1H-indazole-3-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. Its structure is particularly valuable in the development of pharmaceutical agents, especially those targeting enzyme inhibition or receptor modulation. The difluoro substitution on the indazole ring enhances the molecule's ability to interact with specific biological targets, making it a useful building block for drug candidates in areas such as oncology, inflammation, and infectious diseases. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with tailored properties for improved pharmacokinetics and efficacy. This compound is often employed in high-throughput screening and lead optimization processes to identify potential therapeutic molecules.

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inventory 1g
10-20 days ฿19,377.00

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5,6-DIFLUORO-1H-INDAZOLE-3-CARBOXYLIC ACID
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5,6-Difluoro-1H-indazole-3-carboxylic acid is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. Its structure is particularly valuable in the development of pharmaceutical agents, especially those targeting enzyme inhibition or receptor modulation. The difluoro substitution on the indazole ring enhances the molecule's ability to interact with specific biological targets, making it a useful building block for drug candidates in areas such as oncology, inflammation, and infectious diseases. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with tailored properties for improved pharmacokinetics and efficacy. This compound is often employed in high-throughput screening and lead optimization processes to identify potential therapeutic molecules.
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