Rel-(1R,2R)-2-(3-Fluorophenyl)Cyclopropane-1-Carboxylic Acid

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Reagent Code: #231534
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CAS Number 175168-72-6

science Other reagents with same CAS 175168-72-6

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Weight 180.18 g/mol
Formula C₁₀H₉FO₂
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Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its cyclopropane scaffold with defined stereochemistry enhances binding selectivity in drug candidates. Commonly employed in the development of serotonin or dopamine receptor modulators due to the structural rigidity and metabolic stability provided by the fluorinated aryl-cyclopropane motif. Also utilized in asymmetric synthesis routes where stereocontrol is critical for efficacy and safety of the final active ingredient.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,770.00
inventory 250mg
10-20 days ฿6,290.00
inventory 1g
10-20 days ฿21,560.00
inventory 5g
10-20 days ฿79,790.00

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Rel-(1R,2R)-2-(3-Fluorophenyl)Cyclopropane-1-Carboxylic Acid
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Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its cyclopropane scaffold with defined stereochemistry enhances binding selectivity in drug candidates. Commonly employed in the development of serotonin or dopamine receptor modulators due to the structural rigidity and metabolic stability provided by the fluorinated aryl-cyclopropane motif. Also utilized in asymmetric synthesis routes where stereo
Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its cyclopropane scaffold with defined stereochemistry enhances binding selectivity in drug candidates. Commonly employed in the development of serotonin or dopamine receptor modulators due to the structural rigidity and metabolic stability provided by the fluorinated aryl-cyclopropane motif. Also utilized in asymmetric synthesis routes where stereocontrol is critical for efficacy and safety of the final active ingredient.
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