(R)-7-chloro-6-fluorochroman-4-amine

95%

Reagent Code: #228689
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CAS Number 1213054-71-7

science Other reagents with same CAS 1213054-71-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.63 g/mol
Formula C₉H₉ClFNO
badge Registry Numbers
MDL Number MFCD11515407
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key chiral intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the production of advanced antimicrobial agents. Its stereochemistry enhances the binding affinity to bacterial DNA gyrase and topoisomerase IV, improving potency against resistant strains. Employed in pharmaceutical research to develop novel quinolone derivatives with optimized pharmacokinetic profiles and reduced side effects. Also utilized in asymmetric synthesis routes where enantiomeric purity is critical for biological activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿18,490.00
inventory 100mg
10-20 days ฿31,430.00
(R)-7-chloro-6-fluorochroman-4-amine
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Used as a key chiral intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the production of advanced antimicrobial agents. Its stereochemistry enhances the binding affinity to bacterial DNA gyrase and topoisomerase IV, improving potency against resistant strains. Employed in pharmaceutical research to develop novel quinolone derivatives with optimized pharmacokinetic profiles and reduced side effects. Also utilized in asymmetric synthesis routes where enantiomeric purity is criti

Used as a key chiral intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the production of advanced antimicrobial agents. Its stereochemistry enhances the binding affinity to bacterial DNA gyrase and topoisomerase IV, improving potency against resistant strains. Employed in pharmaceutical research to develop novel quinolone derivatives with optimized pharmacokinetic profiles and reduced side effects. Also utilized in asymmetric synthesis routes where enantiomeric purity is critical for biological activity.

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