2-(Azetidin-3-yl)-3-chloro-5-(trifluoromethyl)pyridine

95%

Reagent Code: #41979
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CAS Number 1781241-45-9

science Other reagents with same CAS 1781241-45-9

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Weight 236.6214 g/mol
Formula C₉H₈ClF₃N₂
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MDL Number MFCD28805787
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description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its unique structure, featuring an azetidine ring and a trifluoromethyl group, makes it valuable for developing potential drug candidates, particularly in the area of central nervous system (CNS) disorders. Researchers often explore its derivatives for their potential as receptor modulators or enzyme inhibitors, targeting specific pathways involved in neurological diseases. Additionally, its chloro and trifluoromethyl substituents enhance its binding affinity and metabolic stability, making it a promising scaffold for optimizing pharmacokinetic properties in drug discovery.

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inventory 100mg
10-20 days ฿6,237.00

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2-(Azetidin-3-yl)-3-chloro-5-(trifluoromethyl)pyridine
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its unique structure, featuring an azetidine ring and a trifluoromethyl group, makes it valuable for developing potential drug candidates, particularly in the area of central nervous system (CNS) disorders. Researchers often explore its derivatives for their potential as receptor modulators or enzyme inhibitors, targeting specific pathways involved in neurologic

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its unique structure, featuring an azetidine ring and a trifluoromethyl group, makes it valuable for developing potential drug candidates, particularly in the area of central nervous system (CNS) disorders. Researchers often explore its derivatives for their potential as receptor modulators or enzyme inhibitors, targeting specific pathways involved in neurological diseases. Additionally, its chloro and trifluoromethyl substituents enhance its binding affinity and metabolic stability, making it a promising scaffold for optimizing pharmacokinetic properties in drug discovery.

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