2-(3,5-Di-tert-butyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
- Product Code: 167215
CAS:
1032358-19-2
| Molecular Weight: | 346.31 g./mol | Molecular Formula: | C₂₁H₃₅BO₃ |
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| EC Number: | MDL Number: | MFCD22493891 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its primary role is as a boronic ester derivative, offering enhanced stability and reactivity under palladium-catalyzed conditions. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The tert-butyl and methoxy substituents provide steric bulk and electronic effects that improve selectivity and yield in coupling reactions. Suitable for late-stage functionalization due to its tolerance of various functional groups.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1g | 10-20 days | $1,442.42 |
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| 100mg | 10-20 days | $315.90 |
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2-(3,5-Di-tert-butyl-4-methoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its primary role is as a boronic ester derivative, offering enhanced stability and reactivity under palladium-catalyzed conditions. Commonly employed in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The tert-butyl and methoxy substituents provide steric bulk and electronic effects that improve selectivity and yield in coupling reactions. Suitable for late-stage functionalization due to its tolerance of various functional groups.
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