2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
- Product Code: 41567
CAS:
1256359-13-3
| Molecular Weight: | 310.2200 g./mol | Molecular Formula: | C₁₅H₂₃BO₄S |
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| EC Number: | MDL Number: | MFCD16618963 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a boron-containing reagent, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. The isopropylsulfonyl group enhances its stability and reactivity, allowing for efficient transformations under mild conditions. It is also employed in the development of bioactive compounds and as a building block in medicinal chemistry for drug discovery and optimization. Additionally, its unique structure makes it suitable for use in materials science, particularly in the synthesis of organic electronic materials and polymers.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €30.63 |
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2-(4-(Isopropylsulfonyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
This compound is primarily utilized in organic synthesis as a boron-containing reagent, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, such as pharmaceuticals, agrochemicals, and advanced materials. The isopropylsulfonyl group enhances its stability and reactivity, allowing for efficient transformations under mild conditions. It is also employed in the development of bioactive compounds and as a building block in medicinal chemistry for drug discovery and optimization. Additionally, its unique structure makes it suitable for use in materials science, particularly in the synthesis of organic electronic materials and polymers.
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