2-(Ethoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride)
98%
- Product Code: 89682
CAS:
380430-53-5
| Molecular Weight: | 193.99 g./mol | Molecular Formula: | C₉H₁₁BO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179453 | |
| Melting Point: | 138°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group is essential for coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is utilized in the preparation of biaryl compounds, which are important intermediates in various industrial applications. The presence of the ethoxycarbonyl group enhances its stability and reactivity, making it suitable for diverse synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 97.5 100% |
| Melting point | 136 140? |
| Appearance | Slightly pale yellow - Reddish yellow Crystal - Powder |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿387.00 |
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| 5.000 | 10-20 days | ฿1,206.00 |
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| 25.000 | 10-20 days | ฿5,418.00 |
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2-(Ethoxycarbonyl)phenylboronic Acid (contains varying amounts of Anhydride)
This compound is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key reagent for forming carbon-carbon bonds, enabling the creation of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group is essential for coupling with aryl halides, making it valuable in drug discovery and development. Additionally, it is utilized in the preparation of biaryl compounds, which are important intermediates in various industrial applications. The presence of the ethoxycarbonyl group enhances its stability and reactivity, making it suitable for diverse synthetic pathways.
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