1-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline
95%
- Product Code: 39655
CAS:
1132944-44-5
| Molecular Weight: | 323.2155 g./mol | Molecular Formula: | C₁₅H₂₂BNO₄S |
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| EC Number: | MDL Number: | MFCD28718122 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of bioactive compounds and materials science for creating advanced polymers and functional materials. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $93.44 |
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1-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, it is employed in the development of bioactive compounds and materials science for creating advanced polymers and functional materials. Its stability and reactivity under mild conditions make it a preferred choice in medicinal chemistry for drug discovery and development.
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