6-(Trifluoromethyl)quinolin-8-amine

95%

Reagent Code: #49475
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CAS Number 955413-26-0

science Other reagents with same CAS 955413-26-0

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Weight 212.1700 g/mol
Formula C₁₀H₇F₃N₂
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Storage room temperature

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active compounds. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting molecules, making it valuable in drug development. It is often employed in the creation of potential therapeutic agents targeting diseases such as cancer, inflammation, and infectious diseases. Additionally, its quinoline core structure is advantageous for designing compounds with specific interactions in biological systems, particularly in enzyme inhibition or receptor modulation. Researchers also explore its use in the development of fluorescent probes and imaging agents due to its unique structural properties.

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inventory 100mg
10-20 days ฿9,846.00

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6-(Trifluoromethyl)quinolin-8-amine
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This chemical is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active compounds. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting molecules, making it valuable in drug development. It is often employed in the creation of potential therapeutic agents targeting diseases such as cancer, inflammation, and infectious diseases. Additionally, its quinoline core structure is adv

This chemical is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various biologically active compounds. Its trifluoromethyl group enhances the metabolic stability and bioavailability of the resulting molecules, making it valuable in drug development. It is often employed in the creation of potential therapeutic agents targeting diseases such as cancer, inflammation, and infectious diseases. Additionally, its quinoline core structure is advantageous for designing compounds with specific interactions in biological systems, particularly in enzyme inhibition or receptor modulation. Researchers also explore its use in the development of fluorescent probes and imaging agents due to its unique structural properties.

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