Triisopropyl((6-(methoxymethoxy)-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-yl)ethynyl)silane
97%
- Product Code: 124581
CAS:
2621932-42-9
| Molecular Weight: | 494.55 g./mol | Molecular Formula: | C₂₉H₄₃BO₄Si |
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| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boronic ester intermediate. Its structure, featuring a boronate group and a silyl-protected alkyne, makes it valuable for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. The methoxymethoxy group enhances its stability and reactivity, allowing for selective transformations in multi-step synthetic pathways. Additionally, its naphthalene core is advantageous in the synthesis of conjugated systems, which are essential in the production of organic electronic materials like OLEDs and semiconductors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £78.16 |
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| 0.250 | 10-20 days | £145.13 |
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| 1.000 | 10-20 days | £395.71 |
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Triisopropyl((6-(methoxymethoxy)-8-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-1-yl)ethynyl)silane
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boronic ester intermediate. Its structure, featuring a boronate group and a silyl-protected alkyne, makes it valuable for constructing complex organic molecules, especially in the development of pharmaceuticals and advanced materials. The methoxymethoxy group enhances its stability and reactivity, allowing for selective transformations in multi-step synthetic pathways. Additionally, its naphthalene core is advantageous in the synthesis of conjugated systems, which are essential in the production of organic electronic materials like OLEDs and semiconductors.
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