6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazole
95%
- Product Code: 84688
CAS:
1810038-58-4
| Molecular Weight: | 245.08 g./mol | Molecular Formula: | C₁₃H₁₆BNO₃ |
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| EC Number: | MDL Number: | MFCD13181969 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8 ℃, inert gas storage |
Product Description:
Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds application in material science for creating organic electronic materials and polymers. The benzo[d]oxazole moiety enhances its utility in designing fluorescent probes and sensors for biological and chemical detection. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,051.00 |
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| 0.250 | 10-20 days | ฿4,563.00 |
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| 1.000 | 10-20 days | ฿11,475.00 |
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6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]oxazole
Used extensively in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds application in material science for creating organic electronic materials and polymers. The benzo[d]oxazole moiety enhances its utility in designing fluorescent probes and sensors for biological and chemical detection. Its stability and reactivity under mild conditions make it a preferred choice in various catalytic processes.
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