2-Oxo-2,3-dihydrobenzo[d]oxazole-5-sulfonyl chloride
98%
- Product Code: 222311
CAS:
78633-41-7
| Molecular Weight: | 233.63 g./mol | Molecular Formula: | C₇H₄ClNO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04629624 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its sulfonyl chloride group readily reacts with nucleophiles, enabling efficient formation of sulfonamides, which are common structural motifs in bioactive molecules. It is also employed in the preparation of fluorescent probes and dyes due to the stability and reactivity of the oxazole ring system. In agrochemical research, it serves as a building block for herbicides and insecticides, where the scaffold contributes to enhanced metabolic stability. The compound’s ability to participate in multi-step synthetic routes makes it valuable in medicinal chemistry for lead optimization and library synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,600.00 |
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| 250mg | 10-20 days | ฿3,780.00 |
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| 1g | 10-20 days | ฿10,760.00 |
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2-Oxo-2,3-dihydrobenzo[d]oxazole-5-sulfonyl chloride
Widely used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its sulfonyl chloride group readily reacts with nucleophiles, enabling efficient formation of sulfonamides, which are common structural motifs in bioactive molecules. It is also employed in the preparation of fluorescent probes and dyes due to the stability and reactivity of the oxazole ring system. In agrochemical research, it serves as a building block for herbicides and insecticides, where the scaffold contributes to enhanced metabolic stability. The compound’s ability to participate in multi-step synthetic routes makes it valuable in medicinal chemistry for lead optimization and library synthesis.
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