(R)-5-(2,2-Dimethyl-4H-benzo[d][1,3]dioxin-6-yl)oxazolidin-2-one
≥99%
- Product Code: 37695
CAS:
452339-73-0
| Molecular Weight: | 249.2625 g./mol | Molecular Formula: | C₁₃H₁₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21362968 | |
| Melting Point: | Boiling Point: | 489.6±45.0℃(Predicted) | |
| Density: | 1.223±0.06g/ml(Predicted) | Storage Condition: | 2-8°C, airtight, dry |
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.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿909.00 |
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| 0.250 | 10-20 days | ฿1,908.00 |
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| 1.000 | 10-20 days | ฿5,148.00 |
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(R)-5-(2,2-Dimethyl-4H-benzo[d][1,3]dioxin-6-yl)oxazolidin-2-one
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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