3,3-difluoro-1-[(propan-2-yloxy)carbonyl]cyclobutane-1-carboxylic acid

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Reagent Code: #178991
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CAS Number 1225532-90-0

science Other reagents with same CAS 1225532-90-0

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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated analogs for improved metabolic stability and bioavailability. Its cyclobutane core with difluoro substitution enables modulation of lipophilicity and conformational rigidity, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where fluorine substitution enhances target binding and resistance to oxidative degradation. Also utilized in agrochemical research for designing novel active ingredients with enhanced environmental stability and potency.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,160.00
inventory 1g
10-20 days ฿10,720.00
inventory 5g
10-20 days ฿37,300.00
inventory 10g
10-20 days ฿66,820.00
inventory 250mg
10-20 days ฿4,290.00

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3,3-difluoro-1-[(propan-2-yloxy)carbonyl]cyclobutane-1-carboxylic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated analogs for improved metabolic stability and bioavailability. Its cyclobutane core with difluoro substitution enables modulation of lipophilicity and conformational rigidity, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where fluorine substitution enhances target binding a

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated analogs for improved metabolic stability and bioavailability. Its cyclobutane core with difluoro substitution enables modulation of lipophilicity and conformational rigidity, making it valuable in medicinal chemistry for optimizing drug candidates. Commonly employed in the preparation of protease inhibitors and other bioactive molecules where fluorine substitution enhances target binding and resistance to oxidative degradation. Also utilized in agrochemical research for designing novel active ingredients with enhanced environmental stability and potency.

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