1-methyl-6-(tetramethyl-1, 3, 2-dioxaborolan-2-yl)-2, 3-dihydro-1H-indol-2-one
97%
- Product Code: 196742
CAS:
1428666-17-4
| Molecular Weight: | 273.14 g./mol | Molecular Formula: | C₁₅H₂₀BNO₃ |
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| EC Number: | MDL Number: | MFCD25542038 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, light-proof |
Product Description:
Used in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its indolinone core structure supports the construction of biologically active molecules, particularly in medicinal chemistry for kinase inhibitors and neuroactive compounds. The tetramethyl dioxaborolane group enhances stability and reactivity, making it suitable for late-stage functionalization in complex molecule synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,040.00 |
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| 250mg | 10-20 days | ฿3,990.00 |
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| 1g | 10-20 days | ฿11,400.00 |
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| 5g | 10-20 days | ฿46,550.00 |
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1-methyl-6-(tetramethyl-1, 3, 2-dioxaborolan-2-yl)-2, 3-dihydro-1H-indol-2-one
Used in organic synthesis as a boronic ester reagent for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its indolinone core structure supports the construction of biologically active molecules, particularly in medicinal chemistry for kinase inhibitors and neuroactive compounds. The tetramethyl dioxaborolane group enhances stability and reactivity, making it suitable for late-stage functionalization in complex molecule synthesis.
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