(1S,2S)-2-(trifluoromethyl)cyclobutan-1-aminehydrochloride

98%

Reagent Code: #237668
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CAS Number 2306274-67-7

science Other reagents with same CAS 2306274-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.58 g/mol
Formula C₅H₉ClF₃N
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key chiral building block in pharmaceutical synthesis, particularly in the development of biologically active compounds. Its rigid cyclobutane scaffold and trifluoromethyl group enhance metabolic stability and binding selectivity, making it valuable in drug design for central nervous system agents and protease inhibitors. The amine functionality allows for easy derivatization, enabling incorporation into larger molecules. Commonly employed in asymmetric synthesis routes where stereochemical control is critical for activity. Its hydrochloride salt form improves stability and handling in solid-state reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿25,050.00
(1S,2S)-2-(trifluoromethyl)cyclobutan-1-aminehydrochloride
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Used as a key chiral building block in pharmaceutical synthesis, particularly in the development of biologically active compounds. Its rigid cyclobutane scaffold and trifluoromethyl group enhance metabolic stability and binding selectivity, making it valuable in drug design for central nervous system agents and protease inhibitors. The amine functionality allows for easy derivatization, enabling incorporation into larger molecules. Commonly employed in asymmetric synthesis routes where stereochemical con

Used as a key chiral building block in pharmaceutical synthesis, particularly in the development of biologically active compounds. Its rigid cyclobutane scaffold and trifluoromethyl group enhance metabolic stability and binding selectivity, making it valuable in drug design for central nervous system agents and protease inhibitors. The amine functionality allows for easy derivatization, enabling incorporation into larger molecules. Commonly employed in asymmetric synthesis routes where stereochemical control is critical for activity. Its hydrochloride salt form improves stability and handling in solid-state reactions.

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