2-(2-(Methoxymethoxy)-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
≥98%
- Product Code: 203385
CAS:
517864-11-8
| Molecular Weight: | 278.16 g./mol | Molecular Formula: | C₁₅H₂₃BO₄ |
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| EC Number: | MDL Number: | MFCD22493597 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Inert Gas |
Product Description:
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical development. The methoxymethyl-protected phenol allows for selective deprotection later in synthetic sequences, offering versatility in multi-step routes. Commonly applied in the preparation of bioactive molecules and functional materials requiring precise substitution patterns.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $162.92 |
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| 250mg | 10-20 days | $276.96 |
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| 1g | 10-20 days | $721.21 |
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2-(2-(Methoxymethoxy)-4-methylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as an intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic synthesis. Its boronate ester group facilitates coupling with aryl or vinyl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical development. The methoxymethyl-protected phenol allows for selective deprotection later in synthetic sequences, offering versatility in multi-step routes. Commonly applied in the preparation of bioactive molecules and functional materials requiring precise substitution patterns.
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