5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzodioxole
98%
- Product Code: 241568
CAS:
94838-82-1
| Molecular Weight: | 248.0827 g./mol | Molecular Formula: | C₁₃H₁₇BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05663889 | |
| Melting Point: | 47℃ | Boiling Point: | 337.1℃ at 760 mmHg |
| Density: | 1.15±0.1 g/cm3 | Storage Condition: | 2-8℃ |
Product Description:
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for forming carbon-carbon bonds in organic synthesis. Its boronate ester group enables efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules. It is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and functional materials where precise molecular architecture is required. The presence of the benzodioxole moiety can also contribute to enhanced stability or bioactivity in final products.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $6.20 |
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| 1.000 | 10-20 days | $13.12 |
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| 5.000 | 10-20 days | $36.73 |
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5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-benzodioxole
Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for forming carbon-carbon bonds in organic synthesis. Its boronate ester group enables efficient coupling with aryl or vinyl halides under palladium catalysis, making it valuable in the preparation of complex organic molecules. It is particularly useful in the synthesis of pharmaceuticals, agrochemicals, and functional materials where precise molecular architecture is required. The presence of the benzodioxole moiety can also contribute to enhanced stability or bioactivity in final products.
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