(4-(Morpholinosulfonyl)naphthalen-1-yl)boronic acid
98%
- Product Code: 89268
CAS:
1704082-09-6
| Molecular Weight: | 321.16 g./mol | Molecular Formula: | C₁₄H₁₆BNO₅S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28400448 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its morpholine sulfonyl moiety enhances solubility and stability, which is beneficial in various catalytic processes. This chemical is also explored in the development of fluorescent probes and sensors due to its structural properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿32,140.00 |
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(4-(Morpholinosulfonyl)naphthalen-1-yl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its morpholine sulfonyl moiety enhances solubility and stability, which is beneficial in various catalytic processes. This chemical is also explored in the development of fluorescent probes and sensors due to its structural properties.
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