(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid

97%

Reagent Code: #36251
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CAS Number 515179-19-8

science Other reagents with same CAS 515179-19-8

blur_circular Chemical Specifications

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Weight 180.18 g/mol
Formula C₁₀H₉FO₂
inventory_2 Storage & Handling
Storage room temperature

description Product Description

(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. Its unique cyclopropane ring structure, combined with the presence of a fluorine atom, makes it a valuable intermediate in the synthesis of biologically active compounds. It is often employed in the development of drug candidates, particularly those targeting central nervous system disorders, due to its ability to modulate specific receptors or enzymes. Additionally, its structural features are explored in the design of inhibitors for various enzymes, contributing to the study of metabolic pathways and disease mechanisms. The compound's chiral nature also makes it useful in asymmetric synthesis, enabling the production of enantiomerically pure pharmaceuticals.

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Test Parameter Specification
Purity 96.5-100%
Infrared Spectrum Conforms To Structure
Purity (%) 96.5-100%

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿12,600.00
inventory 100mg
10-20 days ฿6,300.00

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(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid
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(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. Its unique cyclopropane ring structure, combined with the presence of a fluorine atom, makes it a valuable intermediate in the synthesis of biologically active compounds. It is often employed in the development of drug candidates, particularly those targeting central nervous system disorders, due to its ability to modulate specific receptors or enzymes. Additionally, its structural features are explored in the design of inhibitors for various enzymes, contributing to the study of metabolic pathways and disease mechanisms. The compound's chiral nature also makes it useful in asymmetric synthesis, enabling the production of enantiomerically pure pharmaceuticals.
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