(R)-(3-(3-fluoro-4-thiomorpholinophenyl)-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate

95%

Reagent Code: #230938
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CAS Number 168828-73-7

science Other reagents with same CAS 168828-73-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 466.55 g/mol
Formula C₂₁H₂₃FN₂O₅S₂
badge Registry Numbers
MDL Number MFCD31568164
thermostat Physical Properties
Boiling Point 657.7±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.383±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used in pharmaceutical synthesis as a key intermediate in the development of antibacterial agents, particularly in the production of oxazolidinone-class antibiotics. Its structure enables selective reactivity, making it valuable for forming chiral centers in complex drug molecules. Commonly employed in late-stage functionalization due to the presence of the sulfonate leaving group, which facilitates nucleophilic substitution reactions. Also utilized in medicinal chemistry research for optimizing pharmacokinetic properties and improving metabolic stability in candidate drugs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿28,750.00
250mg
10-20 days ฿53,660.00
(R)-(3-(3-fluoro-4-thiomorpholinophenyl)-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate
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Used in pharmaceutical synthesis as a key intermediate in the development of antibacterial agents, particularly in the production of oxazolidinone-class antibiotics. Its structure enables selective reactivity, making it valuable for forming chiral centers in complex drug molecules. Commonly employed in late-stage functionalization due to the presence of the sulfonate leaving group, which facilitates nucleophilic substitution reactions. Also utilized in medicinal chemistry research for optimizing pharmaco

Used in pharmaceutical synthesis as a key intermediate in the development of antibacterial agents, particularly in the production of oxazolidinone-class antibiotics. Its structure enables selective reactivity, making it valuable for forming chiral centers in complex drug molecules. Commonly employed in late-stage functionalization due to the presence of the sulfonate leaving group, which facilitates nucleophilic substitution reactions. Also utilized in medicinal chemistry research for optimizing pharmacokinetic properties and improving metabolic stability in candidate drugs.

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