2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
97%
- Product Code: 116527
CAS:
1294518-25-4
| Molecular Weight: | 268.54 g./mol | Molecular Formula: | C₁₃H₁₈BClO₃ |
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| EC Number: | MDL Number: | MFCD22414580 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules. It is particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura reaction, where it acts as a boron-containing reagent to form carbon-carbon bonds efficiently. This makes it a crucial component in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group provides stability and reactivity, enabling precise control in the synthesis of target compounds. Additionally, it is employed in the production of functionalized aromatic compounds, which are essential in the design of drugs and organic electronic materials.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $114.22 |
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| 0.250 | 10-20 days | $207.38 |
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| 1.000 | 10-20 days | $518.72 |
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2-Chloro-6-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
This chemical is primarily utilized in organic synthesis as a key intermediate in the preparation of complex molecules. It is particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura reaction, where it acts as a boron-containing reagent to form carbon-carbon bonds efficiently. This makes it a crucial component in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronate ester group provides stability and reactivity, enabling precise control in the synthesis of target compounds. Additionally, it is employed in the production of functionalized aromatic compounds, which are essential in the design of drugs and organic electronic materials.
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