3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
98%
- Product Code: 211110
CAS:
1150561-67-3
| Molecular Weight: | 262.11 g./mol | Molecular Formula: | C₁₄H₁₉BO₄ |
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| EC Number: | MDL Number: | MFCD12026101 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boron-containing group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of functional materials. The carboxylic acid functionality allows for further derivatization or attachment to solid supports, enhancing its utility in combinatorial chemistry and library synthesis. Its stability and reactivity profile make it suitable for use in automated synthesis platforms and late-stage functionalization of bioactive compounds.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €17.23 |
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| 0.250 | 10-20 days | €38.96 |
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| 1.000 | 10-20 days | €155.58 |
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| 5.000 | 10-20 days | €777.63 |
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3-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key boronic ester reagent in the synthesis of complex organic molecules, especially in pharmaceutical and agrochemical industries. Its boron-containing group enables efficient carbon-carbon bond formation under mild conditions, making it valuable in drug discovery and development of functional materials. The carboxylic acid functionality allows for further derivatization or attachment to solid supports, enhancing its utility in combinatorial chemistry and library synthesis. Its stability and reactivity profile make it suitable for use in automated synthesis platforms and late-stage functionalization of bioactive compounds.
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