2,2,2-Trifluoroacetic acid compound with (4-(1-(piperazin-1-yl)ethyl)phenyl)boronic acid (1:1)
98%
- Product Code: 89222
CAS:
1704069-49-7
| Molecular Weight: | 348.13 g./mol | Molecular Formula: | C₁₄H₂₀BF₃N₂O₄ |
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| EC Number: | MDL Number: | MFCD28384347 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique chemical properties. It serves as a key intermediate in the development of boron-containing molecules, which are widely explored in medicinal chemistry for their potential therapeutic applications. The trifluoroacetic acid component enhances reactivity and stability, making it valuable in peptide synthesis and as a catalyst in various chemical reactions. Additionally, the boronic acid moiety is crucial in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Its application extends to the preparation of bioactive compounds, particularly in the development of enzyme inhibitors and receptor modulators, contributing to advancements in targeted therapies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿28,660.00 |
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2,2,2-Trifluoroacetic acid compound with (4-(1-(piperazin-1-yl)ethyl)phenyl)boronic acid (1:1)
This compound is primarily utilized in organic synthesis and pharmaceutical research due to its unique chemical properties. It serves as a key intermediate in the development of boron-containing molecules, which are widely explored in medicinal chemistry for their potential therapeutic applications. The trifluoroacetic acid component enhances reactivity and stability, making it valuable in peptide synthesis and as a catalyst in various chemical reactions. Additionally, the boronic acid moiety is crucial in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in drug discovery and material science. Its application extends to the preparation of bioactive compounds, particularly in the development of enzyme inhibitors and receptor modulators, contributing to advancements in targeted therapies.
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