4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl carbonochloridate
97%
- Product Code: 244089
CAS:
1334019-92-9
| Molecular Weight: | 296.55 g./mol | Molecular Formula: | C₁₄H₁₈BClO₄ |
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| EC Number: | MDL Number: | MFCD34168998 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used primarily as a reagent in organic synthesis, especially in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a boronate ester precursor. The compound enables the formation of biaryl structures by reacting with aryl halides in the presence of a palladium catalyst. Its carbonochloridate group allows for further functionalization, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. It is particularly useful in multi-step syntheses where selective and efficient bond formation is required. Due to its reactivity, it is handled under anhydrous conditions and inert atmosphere to prevent decomposition.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $150.55 |
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| 0.250 | 10-20 days | $255.17 |
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| 1.000 | 10-20 days | $832.70 |
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| 5.000 | 10-20 days | $2,208.05 |
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| 25.000 | 10-20 days | $9,645.35 |
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl carbonochloridate
Used primarily as a reagent in organic synthesis, especially in cross-coupling reactions such as Suzuki-Miyaura coupling, where it serves as a boronate ester precursor. The compound enables the formation of biaryl structures by reacting with aryl halides in the presence of a palladium catalyst. Its carbonochloridate group allows for further functionalization, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and complex organic molecules. It is particularly useful in multi-step syntheses where selective and efficient bond formation is required. Due to its reactivity, it is handled under anhydrous conditions and inert atmosphere to prevent decomposition.
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