(S)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl-3,3'-diboronic Acid Pinacol Ester
≥98%,99%e.e.
- Product Code: 70474
CAS:
260441-99-4
| Molecular Weight: | 626.4 g./mol | Molecular Formula: | C₃₆H₄₄B₂O₈ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 196-197°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
(S)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl-3,3'-diboronic Acid Pinacol Ester is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands and catalysts. Its structure makes it valuable in enantioselective reactions, such as the Suzuki-Miyaura cross-coupling, where it aids in forming carbon-carbon bonds with high stereochemical control. This compound is also employed in the synthesis of complex organic molecules, including pharmaceuticals, where chirality plays a critical role in biological activity. Additionally, it serves as a key intermediate in the preparation of advanced materials and chiral frameworks for use in molecular recognition and sensor technologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿21,880.00 |
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(S)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl-3,3'-diboronic Acid Pinacol Ester
(S)-2,2'-Bis(methoxymethoxy)-1,1'-binaphthyl-3,3'-diboronic Acid Pinacol Ester is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands and catalysts. Its structure makes it valuable in enantioselective reactions, such as the Suzuki-Miyaura cross-coupling, where it aids in forming carbon-carbon bonds with high stereochemical control. This compound is also employed in the synthesis of complex organic molecules, including pharmaceuticals, where chirality plays a critical role in biological activity. Additionally, it serves as a key intermediate in the preparation of advanced materials and chiral frameworks for use in molecular recognition and sensor technologies.
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