2-(Tributylstannyl)oxazole
95%
- Product Code: 42348
CAS:
145214-05-7
| Molecular Weight: | 358.1069 g./mol | Molecular Formula: | C₁₅H₂₉NOSn |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06798076 | |
| Melting Point: | 227-228 °C | Boiling Point: | 108-110 °C at 760 mmHg |
| Density: | 1.71 g/cm3 | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, this compound serves as a key reagent in the formation of carbon-carbon and carbon-heteroatom bonds. It is particularly valuable in Stille coupling reactions, where it facilitates the cross-coupling of organostannanes with organic halides or pseudohalides to construct complex molecules. This makes it essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its oxazole moiety is often leveraged in the development of bioactive compounds, including antimicrobial and anticancer agents. Its role in synthesizing heterocyclic compounds further enhances its utility in drug discovery and material science.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | colorless liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £77.80 |
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| 0.250 | 10-20 days | £157.87 |
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| 1.000 | 10-20 days | £517.48 |
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2-(Tributylstannyl)oxazole
Used primarily in organic synthesis, this compound serves as a key reagent in the formation of carbon-carbon and carbon-heteroatom bonds. It is particularly valuable in Stille coupling reactions, where it facilitates the cross-coupling of organostannanes with organic halides or pseudohalides to construct complex molecules. This makes it essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its oxazole moiety is often leveraged in the development of bioactive compounds, including antimicrobial and anticancer agents. Its role in synthesizing heterocyclic compounds further enhances its utility in drug discovery and material science.
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