3,3-Difluorocyclobutanecarboxylic Acid

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Reagent Code: #174245
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CAS Number 107496-54-8

science Other reagents with same CAS 107496-54-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 136.10 g/mol
Formula C₅H₆F₂O₂
badge Registry Numbers
MDL Number MFCD08705857
thermostat Physical Properties
Melting Point 53°C
Boiling Point 205°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key building block in pharmaceutical synthesis, particularly in the development of biologically active compounds. Its rigid cyclobutane structure and fluorine substitutions enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where fluorination improves pharmacokinetic properties. Also utilized in agrochemicals for creating structurally constrained intermediates that increase selectivity and efficacy. The carboxylic acid group allows for easy derivatization, enabling peptide coupling and ester formation in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿420.00
inventory 5g
10-20 days ฿1,490.00
inventory 25g
10-20 days ฿7,000.00
inventory 100g
10-20 days ฿27,770.00

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3,3-Difluorocyclobutanecarboxylic Acid
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Used as a key building block in pharmaceutical synthesis, particularly in the development of biologically active compounds. Its rigid cyclobutane structure and fluorine substitutions enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where fluorination improves pharmacokinetic properties. Also utilized in agrochemicals for creating structurally constrained intermediates that increase selectivity and

Used as a key building block in pharmaceutical synthesis, particularly in the development of biologically active compounds. Its rigid cyclobutane structure and fluorine substitutions enhance metabolic stability and binding affinity in drug candidates. Commonly employed in the preparation of protease inhibitors and other therapeutic agents where fluorination improves pharmacokinetic properties. Also utilized in agrochemicals for creating structurally constrained intermediates that increase selectivity and efficacy. The carboxylic acid group allows for easy derivatization, enabling peptide coupling and ester formation in multi-step syntheses.

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