1-Methyl-4-(2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)piperazine
95%
- Product Code: 83493
CAS:
2246691-45-0
| Molecular Weight: | 346.27204 g./mol | Molecular Formula: | C₁₉H₃₁BN₂O₃ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a piperazine ring and a boronate ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the creation of complex organic compounds. This reaction is essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound's boronate ester moiety allows it to act as a protecting group or a functional handle in organic synthesis, enabling the precise construction of target molecules. Its application is particularly significant in the development of potential therapeutic agents, including those targeting neurological disorders and cancer.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿7,974.00 |
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| 0.250 | 10-20 days | ฿23,976.00 |
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1-Methyl-4-(2-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)ethyl)piperazine
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a piperazine ring and a boronate ester group, makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the creation of complex organic compounds. This reaction is essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound's boronate ester moiety allows it to act as a protecting group or a functional handle in organic synthesis, enabling the precise construction of target molecules. Its application is particularly significant in the development of potential therapeutic agents, including those targeting neurological disorders and cancer.
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