4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-3-CYCLOHEXENE-1-CARBOXYLIC ACID METHYL ESTER
97%
- Product Code: 240426
CAS:
151075-20-6
| Molecular Weight: | 266.14 g./mol | Molecular Formula: | C₁₄H₂₃BO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃, dry, sealed |
Product Description:
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed reactions, making it valuable for constructing complex organic molecules, especially in drug discovery and development. The presence of a methyl ester allows for further functionalization, enhancing its utility in multi-step synthetic routes. It is particularly favored in research settings for creating substituted cyclohexene derivatives with high stereochemical control.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $27.21 |
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| 0.250 | 10-20 days | $55.03 |
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| 1.000 | 10-20 days | $164.79 |
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| 5.000 | 10-20 days | $659.46 |
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| 10.000 | 10-20 days | $1,187.21 |
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4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-3-CYCLOHEXENE-1-CARBOXYLIC ACID METHYL ESTER
Used primarily as a key intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed reactions, making it valuable for constructing complex organic molecules, especially in drug discovery and development. The presence of a methyl ester allows for further functionalization, enhancing its utility in multi-step synthetic routes. It is particularly favored in research settings for creating substituted cyclohexene derivatives with high stereochemical control.
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