2-(cyclopentylidenemethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
98%
- Product Code: 162437
CAS:
167693-19-8
| Molecular Weight: | 208.11 g./mol | Molecular Formula: | C₁₂H₂₁BO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce alkenyl or aryl groups, enabling the formation of carbon-carbon bonds in pharmaceuticals, agrochemicals, and advanced materials. The cyclopentylidene moiety allows access to strained or conformationally restricted structures, which are valuable in drug design for enhancing metabolic stability and target selectivity. Its stability and reactivity profile make it suitable for late-stage functionalization in complex molecule synthesis.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow solid |
| Purity (%) | 98-100 |
| Infrared Spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | Ft18,914.89 |
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| 0.500 | 10-20 days | Ft128,621.24 |
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| 1.000 | 10-20 days | Ft192,301.36 |
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2-(cyclopentylidenemethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Used as a key reagent in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boron-based coupling partner to introduce alkenyl or aryl groups, enabling the formation of carbon-carbon bonds in pharmaceuticals, agrochemicals, and advanced materials. The cyclopentylidene moiety allows access to strained or conformationally restricted structures, which are valuable in drug design for enhancing metabolic stability and target selectivity. Its stability and reactivity profile make it suitable for late-stage functionalization in complex molecule synthesis.
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| Stable in pH range | - |
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