1-(4-(trifluoromethoxy)phenyl)cyclobutane-1-carboxylic acid

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Reagent Code: #241962
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CAS Number 151157-53-8

science Other reagents with same CAS 151157-53-8

blur_circular Chemical Specifications

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Weight 260.21 g/mol
Formula C₁₂H₁₁F₃O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. The cyclobutane ring and trifluoromethoxy-substituted phenyl moiety enhance cell membrane permeability and biological target specificity. Its structure supports the modulation of receptor activity, making it valuable in creating analogs for neuroactive drugs. The compound's stability and functional group compatibility allow for efficient derivatization in medicinal chemistry workflows. It is also employed in the preparation of selective enzyme inhibitors due to its ability to enhance binding affinity and metabolic resistance in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,470.00
inventory 250mg
10-20 days ฿5,560.00
inventory 1g
10-20 days ฿13,940.00

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1-(4-(trifluoromethoxy)phenyl)cyclobutane-1-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. The cyclobutane ring and trifluoromethoxy-substituted phenyl moiety enhance cell membrane permeability and biological target specificity. Its structure supports the modulation of receptor activity, making it valuable in creating analogs for neuroactive drugs. The compound's stability and functional group compatibility allow for efficient derivatization in medici

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of central nervous system (CNS) agents. The cyclobutane ring and trifluoromethoxy-substituted phenyl moiety enhance cell membrane permeability and biological target specificity. Its structure supports the modulation of receptor activity, making it valuable in creating analogs for neuroactive drugs. The compound's stability and functional group compatibility allow for efficient derivatization in medicinal chemistry workflows. It is also employed in the preparation of selective enzyme inhibitors due to its ability to enhance binding affinity and metabolic resistance in drug candidates.

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