(S)-5-(Aminomethyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one

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Reagent Code: #234990
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CAS Number 168828-90-8

science Other reagents with same CAS 168828-90-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.31 g/mol
Formula C₁₄H₁₈FN₃O₃
badge Registry Numbers
MDL Number MFCD18379308
thermostat Physical Properties
Boiling Point 480°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of linezolid, a synthetic antibiotic effective against Gram-positive bacteria, including multidrug-resistant strains such as MRSA and vancomycin-resistant enterococci (VRE). Its structure enables inhibition of bacterial protein synthesis by binding to the 23S ribosomal RNA of the 50S subunit, making it valuable in treating severe infections like pneumonia, skin infections, and bacteremia. Due to its stereochemistry, the (S)-enantiomer is crucial for maintaining high antibacterial activity and minimizing off-target effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿126.50
inventory 500mg
10-20 days ฿860.00
inventory 5g
10-20 days ฿1,260.00
inventory 25g
10-20 days ฿5,110.00
inventory 100g
10-20 days ฿20,370.00

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(S)-5-(Aminomethyl)-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one
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Used as a key intermediate in the synthesis of linezolid, a synthetic antibiotic effective against Gram-positive bacteria, including multidrug-resistant strains such as MRSA and vancomycin-resistant enterococci (VRE). Its structure enables inhibition of bacterial protein synthesis by binding to the 23S ribosomal RNA of the 50S subunit, making it valuable in treating severe infections like pneumonia, skin infections, and bacteremia. Due to its stereochemistry, the (S)-enantiomer is crucial for maintaining

Used as a key intermediate in the synthesis of linezolid, a synthetic antibiotic effective against Gram-positive bacteria, including multidrug-resistant strains such as MRSA and vancomycin-resistant enterococci (VRE). Its structure enables inhibition of bacterial protein synthesis by binding to the 23S ribosomal RNA of the 50S subunit, making it valuable in treating severe infections like pneumonia, skin infections, and bacteremia. Due to its stereochemistry, the (S)-enantiomer is crucial for maintaining high antibacterial activity and minimizing off-target effects.

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