(R)-3-(3-Fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-one

98%

Reagent Code: #229856
label
Alias (R)-3-(3-fluorophenyl)-5-hydroxymethyloxazolidin-2-one
fingerprint
CAS Number 149524-42-5

science Other reagents with same CAS 149524-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.19 g/mol
Formula C₁₀H₁₀FNO₃
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key chiral intermediate in the synthesis of antibacterial agents, particularly in the production of linezolid and related oxazolidinone-class antibiotics. Its stereochemistry enables effective inhibition of bacterial protein synthesis, making it valuable in developing potent antimicrobial drugs. The hydroxymethyl and fluorophenyl groups contribute to enhanced bioavailability and binding affinity to the bacterial ribosome. Widely utilized in pharmaceutical research for optimizing novel antibiotics targeting drug-resistant strains such as MRSA and vancomycin-resistant enterococci.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿174.00
inventory 250mg
10-20 days ฿192.50
inventory 1g
10-20 days ฿1,330.00
inventory 5g
10-20 days ฿6,340.00
(R)-3-(3-Fluorophenyl)-5-(hydroxymethyl)oxazolidin-2-one
No image available

Used as a key chiral intermediate in the synthesis of antibacterial agents, particularly in the production of linezolid and related oxazolidinone-class antibiotics. Its stereochemistry enables effective inhibition of bacterial protein synthesis, making it valuable in developing potent antimicrobial drugs. The hydroxymethyl and fluorophenyl groups contribute to enhanced bioavailability and binding affinity to the bacterial ribosome. Widely utilized in pharmaceutical research for optimizing novel antibioti

Used as a key chiral intermediate in the synthesis of antibacterial agents, particularly in the production of linezolid and related oxazolidinone-class antibiotics. Its stereochemistry enables effective inhibition of bacterial protein synthesis, making it valuable in developing potent antimicrobial drugs. The hydroxymethyl and fluorophenyl groups contribute to enhanced bioavailability and binding affinity to the bacterial ribosome. Widely utilized in pharmaceutical research for optimizing novel antibiotics targeting drug-resistant strains such as MRSA and vancomycin-resistant enterococci.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...