1-(2-(2-Chloro-3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)-4-methylpiperazine
97%
- Product Code: 39159
CAS:
1799612-11-5
| Molecular Weight: | 394.74 g./mol | Molecular Formula: | C₂₀H₃₂BClN₂O₃ |
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| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex organic molecules. The presence of the piperazine moiety also suggests potential applications in the design of bioactive compounds, as piperazine derivatives are often incorporated into drugs targeting the central nervous system, such as antipsychotics and antidepressants. Additionally, the chloro and methyl groups on the aromatic ring may contribute to the compound's reactivity and selectivity in various chemical transformations, making it a versatile building block in medicinal chemistry and drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,871.00 |
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| 0.250 | 10-20 days | ฿4,878.00 |
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| 1.000 | 10-20 days | ฿13,167.00 |
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1-(2-(2-Chloro-3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)-4-methylpiperazine
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring a dioxaborolane group, makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in complex organic molecules. The presence of the piperazine moiety also suggests potential applications in the design of bioactive compounds, as piperazine derivatives are often incorporated into drugs targeting the central nervous system, such as antipsychotics and antidepressants. Additionally, the chloro and methyl groups on the aromatic ring may contribute to the compound's reactivity and selectivity in various chemical transformations, making it a versatile building block in medicinal chemistry and drug discovery.
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