(S)-(2-Oxooxazolidin-4-yl)methyl 4-methylbenzenesulfonate

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Reagent Code: #236553
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CAS Number 154669-49-5

science Other reagents with same CAS 154669-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.29 g/mol
Formula C₁₁H₁₃NO₅S
badge Registry Numbers
MDL Number MFCD20483424
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral intermediate, specifically the (S)-isomer, in the synthesis of antibacterial agents, particularly in the production of oxazolidinone-class antibiotics like linezolid and tedizolid. These antibiotics target gram-positive resistant bacteria, such as MRSA and VRE. Its stereochemistry enables selective reactions in asymmetric synthesis, making it valuable in pharmaceutical development. It plays a crucial role in carbon-carbon bond formation or functional group addition at specific molecular positions, ideal for laboratory drug development requiring high (S)-isomer purity. Commonly employed to introduce activated chiral building blocks in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿400.00
inventory 250mg
10-20 days ฿730.00
inventory 1g
10-20 days ฿2,580.00
(S)-(2-Oxooxazolidin-4-yl)methyl 4-methylbenzenesulfonate
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Used as a chiral intermediate, specifically the (S)-isomer, in the synthesis of antibacterial agents, particularly in the production of oxazolidinone-class antibiotics like linezolid and tedizolid. These antibiotics target gram-positive resistant bacteria, such as MRSA and VRE. Its stereochemistry enables selective reactions in asymmetric synthesis, making it valuable in pharmaceutical development. It plays a crucial role in carbon-carbon bond formation or functional group addition at specific molecular

Used as a chiral intermediate, specifically the (S)-isomer, in the synthesis of antibacterial agents, particularly in the production of oxazolidinone-class antibiotics like linezolid and tedizolid. These antibiotics target gram-positive resistant bacteria, such as MRSA and VRE. Its stereochemistry enables selective reactions in asymmetric synthesis, making it valuable in pharmaceutical development. It plays a crucial role in carbon-carbon bond formation or functional group addition at specific molecular positions, ideal for laboratory drug development requiring high (S)-isomer purity. Commonly employed to introduce activated chiral building blocks in complex molecule assembly.

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