(5R)-3-(3-Fluoro-4-(4-morpholinyl)phenyl)-5-hydroxymethyl-2-oxazolidione

98%

Reagent Code: #229966
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CAS Number 168828-82-8

science Other reagents with same CAS 168828-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.30 g/mol
Formula C₁₄H₁₇FN₂O₄
badge Registry Numbers
MDL Number MFCD06658241
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This compound is a key intermediate in the synthesis of oxazolidinone-class antibiotics, such as Linezolid, used for treating serious Gram-positive bacterial infections, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). The 5-hydroxymethyl group serves as a functional handle for further derivatization in the manufacturing process. Its structure, featuring a 3-fluoro-4-morpholinophenyl substituent, contributes to the antibacterial potency and selectivity of the final drug by targeting bacterial protein synthesis at the ribosome.

Additionally, derivatives of this oxazolidinone scaffold are investigated for broader antimicrobial applications, potential immunomodulatory effects, and uses in oncology or autoimmune disease research due to their unique binding properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿430.00
inventory 5g
10-20 days ฿920.00
inventory 25g
10-20 days ฿1,908.50
inventory 100g
10-20 days ฿12,460.00
(5R)-3-(3-Fluoro-4-(4-morpholinyl)phenyl)-5-hydroxymethyl-2-oxazolidione
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This compound is a key intermediate in the synthesis of oxazolidinone-class antibiotics, such as Linezolid, used for treating serious Gram-positive bacterial infections, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). The 5-hydroxymethyl group serves as a functional handle for further derivatization in the manufacturing process. Its structure, featuring a 3-fluoro-4-morpholinophenyl substituent, contributes to the antibacterial potency and selecti

This compound is a key intermediate in the synthesis of oxazolidinone-class antibiotics, such as Linezolid, used for treating serious Gram-positive bacterial infections, including methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant Enterococcus (VRE). The 5-hydroxymethyl group serves as a functional handle for further derivatization in the manufacturing process. Its structure, featuring a 3-fluoro-4-morpholinophenyl substituent, contributes to the antibacterial potency and selectivity of the final drug by targeting bacterial protein synthesis at the ribosome.

Additionally, derivatives of this oxazolidinone scaffold are investigated for broader antimicrobial applications, potential immunomodulatory effects, and uses in oncology or autoimmune disease research due to their unique binding properties.

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