benzo[d]oxazol-4-yl trifluoromethanesulfonate
95%
- Product Code: 83059
CAS:
177734-80-4
| Molecular Weight: | 267.18 g./mol | Molecular Formula: | C₈H₄F₃NO₄S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31652574 | |
| Melting Point: | Boiling Point: | 315.1±42.0 °C(Predicted) | |
| Density: | 1.659±0.06 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile reagent for introducing the benzo[d]oxazole moiety into various molecular structures. Its trifluoromethanesulfonate group acts as an excellent leaving group, facilitating efficient coupling reactions, particularly in cross-coupling processes such as Suzuki or Sonogashira reactions. It is also employed in the development of pharmaceuticals and agrochemicals, where the benzo[d]oxazole scaffold is valued for its biological activity. Additionally, it serves as a key intermediate in the synthesis of complex organic compounds, including heterocyclic frameworks, which are essential in material science and medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,115.00 |
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| 0.250 | 10-20 days | ฿20,475.00 |
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| 1.000 | 10-20 days | ฿40,950.00 |
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benzo[d]oxazol-4-yl trifluoromethanesulfonate
This chemical is primarily utilized in organic synthesis as a versatile reagent for introducing the benzo[d]oxazole moiety into various molecular structures. Its trifluoromethanesulfonate group acts as an excellent leaving group, facilitating efficient coupling reactions, particularly in cross-coupling processes such as Suzuki or Sonogashira reactions. It is also employed in the development of pharmaceuticals and agrochemicals, where the benzo[d]oxazole scaffold is valued for its biological activity. Additionally, it serves as a key intermediate in the synthesis of complex organic compounds, including heterocyclic frameworks, which are essential in material science and medicinal chemistry research.
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