(S)-5-Fluoro-3-methylisobenzofuran-1(3H)-one

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Reagent Code: #233619
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CAS Number 1803573-19-4

science Other reagents with same CAS 1803573-19-4

blur_circular Chemical Specifications

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Weight 166.15 g/mol
Formula C₉H₇FO₂
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MDL Number MFCD32660832
inventory_2 Storage & Handling
Storage Room temperature, dry

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 fluorinated structure enhances metabolic stability and bioavailability, making it valuable in developing selective serotonin reuptake inhibitors (SSRIs) and related antidepressant drugs. The compound’s stereochemistry allows for precise interaction with enzymatic targets, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where high enantiomeric purity is required for optimal therapeutic performance.

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inventory 1g
10-20 days ฿1,220.00

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(S)-5-Fluoro-3-methylisobenzofuran-1(3H)-one
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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 fluorinated structure enhances metabolic stability and bioavailability, making it valuable in developing selective serotonin reuptake inhibitors (SSRIs) and related antidepressant drugs. The compound’s stereochemistry allows for precise interaction with enzymatic targets, improving drug efficacy and reducing side effects. Commonly employed in

Used as a key chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. Its fluorinated structure enhances metabolic stability and bioavailability, making it valuable in developing selective serotonin reuptake inhibitors (SSRIs) and related antidepressant drugs. The compound’s stereochemistry allows for precise interaction with enzymatic targets, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where high enantiomeric purity is required for optimal therapeutic performance.

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