1-(3,4,5-trifluorophenyl)cyclopropan-1-amine hydrochloride

98%

Reagent Code: #242118
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CAS Number 1248300-11-9

science Other reagents with same CAS 1248300-11-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.62 g/mol
Formula C₉H₉ClF₃N
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of fluorinated analogs of bioactive molecules. Its rigid cyclopropane scaffold combined with fluorinated aromatic substitution enhances metabolic stability and binding selectivity, making it valuable in medicinal chemistry for CNS-targeted drugs and kinase inhibitors. The amine functionality allows for facile derivatization, enabling incorporation into larger molecular architectures for structure-activity relationship studies. Also employed in the preparation of fluorinated building blocks for PET tracer development due to the presence of multiple fluorine atoms that can aid in imaging applications.

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inventory 250mg
10-20 days ฿16,610.00

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1-(3,4,5-trifluorophenyl)cyclopropan-1-amine hydrochloride
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of fluorinated analogs of bioactive molecules. Its rigid cyclopropane scaffold combined with fluorinated aromatic substitution enhances metabolic stability and binding selectivity, making it valuable in medicinal chemistry for CNS-targeted drugs and kinase inhibitors. The amine functionality allows for facile derivatization, enabling incorporation into larger molecular architectures for structure-activit

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of fluorinated analogs of bioactive molecules. Its rigid cyclopropane scaffold combined with fluorinated aromatic substitution enhances metabolic stability and binding selectivity, making it valuable in medicinal chemistry for CNS-targeted drugs and kinase inhibitors. The amine functionality allows for facile derivatization, enabling incorporation into larger molecular architectures for structure-activity relationship studies. Also employed in the preparation of fluorinated building blocks for PET tracer development due to the presence of multiple fluorine atoms that can aid in imaging applications.

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