(R)-5-(2,2-Dimethyl-4H-benzo[d][1,3]dioxin-6-yl)oxazolidin-2-one

≥99%

Reagent Code: #37695
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CAS Number 452339-73-0

science Other reagents with same CAS 452339-73-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.2625 g/mol
Formula C₁₃H₁₅NO₄
badge Registry Numbers
MDL Number MFCD21362968
thermostat Physical Properties
Boiling Point 489.6±45.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.223±0.06g/ml(Predicted)
Storage 2-8°C, airtight, dry

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of chiral drugs. Its structure, featuring an oxazolidinone ring, is particularly valuable in the development of antibiotics and antimicrobial agents. The compound's stereochemistry plays a crucial role in enhancing the efficacy and selectivity of the resulting drugs. Additionally, it is employed in research settings for studying enzyme interactions and designing novel therapeutic agents targeting bacterial infections. Its application extends to the development of treatments for resistant strains of bacteria, contributing to advancements in combating antibiotic resistance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,148.00
inventory 50mg
10-20 days ฿909.00
inventory 250mg
10-20 days ฿1,908.00

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(R)-5-(2,2-Dimethyl-4H-benzo[d][1,3]dioxin-6-yl)oxazolidin-2-one
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This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of chiral drugs. Its structure, featuring an oxazolidinone ring, is particularly valuable in the development of antibiotics and antimicrobial agents. The compound's stereochemistry plays a crucial role in enhancing the efficacy and selectivity of the resulting drugs. Additionally, it is employed in research settings for studying enzyme interactions and designing novel therapeutic agents targeting bac

This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of chiral drugs. Its structure, featuring an oxazolidinone ring, is particularly valuable in the development of antibiotics and antimicrobial agents. The compound's stereochemistry plays a crucial role in enhancing the efficacy and selectivity of the resulting drugs. Additionally, it is employed in research settings for studying enzyme interactions and designing novel therapeutic agents targeting bacterial infections. Its application extends to the development of treatments for resistant strains of bacteria, contributing to advancements in combating antibiotic resistance.

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