4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
98%
- Product Code: 203140
Alias:
-Methyl-5-hydroxybenzene boric acid Pinna alcohol ester; 5-hydroxy-2-methylbenzene boric acid Pinna alcohol ester; 2-(5-hydroxy-2-methylphenyl) boric acid Pinna alcohol ester; 2-(5-hydroxy-2-methylphenyl) boric acid Pinna alcohol ester
CAS:
1196985-65-5
Molecular Weight: | 234.10 g./mol | Molecular Formula: | C₁₃H₁₉BO₃ |
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EC Number: | MDL Number: | MFCD16994425 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is particularly valuable in the preparation of biaryl compounds and functionalized phenols used in drug development and materials science. The presence of a phenolic hydroxyl group also allows for further derivatization, enhancing its utility in multi-step synthetic routes.
Sizes / Availability / Pricing:
Size | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿6,450.00 |
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1.000 | 10-20 days | ฿20,750.00 |
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4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of carbon-carbon bonds under mild conditions. It is particularly valuable in the preparation of biaryl compounds and functionalized phenols used in drug development and materials science. The presence of a phenolic hydroxyl group also allows for further derivatization, enhancing its utility in multi-step synthetic routes.
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