Tert-butyldimethyl((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl)oxy)silane
98%
- Product Code: 57696
CAS:
865869-27-8
| Molecular Weight: | 338.37 g./mol | Molecular Formula: | C₁₈H₃₅BO₃Si |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11618142 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, store under inert gas |
Product Description:
This compound is primarily used in organic synthesis as a protecting group for alcohols and as a key intermediate in the preparation of complex molecules. Its silicon-based structure allows it to selectively protect hydroxyl groups during multi-step reactions, ensuring that specific functional groups remain unaffected. Additionally, the boronate ester moiety in the molecule makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a versatile tool in the development of novel organic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,212.00 |
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| 0.250 | 10-20 days | ฿7,920.00 |
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| 1.000 | 10-20 days | ฿19,692.00 |
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Tert-butyldimethyl((4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-en-1-yl)oxy)silane
This compound is primarily used in organic synthesis as a protecting group for alcohols and as a key intermediate in the preparation of complex molecules. Its silicon-based structure allows it to selectively protect hydroxyl groups during multi-step reactions, ensuring that specific functional groups remain unaffected. Additionally, the boronate ester moiety in the molecule makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity make it a versatile tool in the development of novel organic compounds.
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