6-Chloro-4-fluoro-3-iodo-1H-indazole

95%

Reagent Code: #49760
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CAS Number 887567-96-6

science Other reagents with same CAS 887567-96-6

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Weight 296.4680 g/mol
Formula C₇H₃ClFIN₂
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description Product Description

6-Chloro-4-fluoro-3-iodo-1H-indazole is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its unique halogenated structure makes it valuable for designing and optimizing drug candidates, particularly in the development of kinase inhibitors and other therapeutic agents targeting specific enzymes or proteins. The compound is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and enhance the potency, selectivity, and pharmacokinetic properties of potential drugs. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules for further biological evaluation. Its applications are particularly prominent in the fields of oncology and inflammation, where it contributes to the discovery of novel treatments.

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inventory 100mg
10-20 days ฿2,241.00

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6-Chloro-4-fluoro-3-iodo-1H-indazole
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6-Chloro-4-fluoro-3-iodo-1H-indazole is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its unique halogenated structure makes it valuable for designing and optimizing drug candidates, particularly in the development of kinase inhibitors and other therapeutic agents targeting specific enzymes or proteins. The compound is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and

6-Chloro-4-fluoro-3-iodo-1H-indazole is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its unique halogenated structure makes it valuable for designing and optimizing drug candidates, particularly in the development of kinase inhibitors and other therapeutic agents targeting specific enzymes or proteins. The compound is often employed in medicinal chemistry to explore structure-activity relationships (SAR) and enhance the potency, selectivity, and pharmacokinetic properties of potential drugs. Additionally, it serves as a building block in organic synthesis, enabling the creation of complex molecules for further biological evaluation. Its applications are particularly prominent in the fields of oncology and inflammation, where it contributes to the discovery of novel treatments.

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