3-Pentyn-2-ol
≥98.0% (GC)
- Product Code: 57453
CAS:
58072-60-9
| Molecular Weight: | 84.12 g./mol | Molecular Formula: | C₅H₈O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00046652 | |
| Melting Point: | -24.1°C (estimate) | Boiling Point: | 138-140℃ (lit.) |
| Density: | 0.900 g/mL at 20℃ (lit.) | Storage Condition: | 2-8℃ |
Product Description:
3-Pentyn-2-ol is primarily used in organic synthesis as a building block for more complex chemical compounds. Its structure, featuring both an alkyne and a hydroxyl group, makes it versatile in various chemical reactions. It is often employed in the preparation of pharmaceuticals, where it can serve as an intermediate in the synthesis of active pharmaceutical ingredients (APIs). Additionally, it is utilized in the development of specialty chemicals, including agrochemicals and polymers, where its reactive groups can be modified to achieve desired properties. In research, 3-Pentyn-2-ol is used to study reaction mechanisms and to develop new synthetic methodologies, particularly in the field of click chemistry. Its ability to participate in alkyne-based reactions, such as cycloadditions, makes it valuable for creating complex molecular architectures efficiently.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿5,913.00 |
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3-Pentyn-2-ol
3-Pentyn-2-ol is primarily used in organic synthesis as a building block for more complex chemical compounds. Its structure, featuring both an alkyne and a hydroxyl group, makes it versatile in various chemical reactions. It is often employed in the preparation of pharmaceuticals, where it can serve as an intermediate in the synthesis of active pharmaceutical ingredients (APIs). Additionally, it is utilized in the development of specialty chemicals, including agrochemicals and polymers, where its reactive groups can be modified to achieve desired properties. In research, 3-Pentyn-2-ol is used to study reaction mechanisms and to develop new synthetic methodologies, particularly in the field of click chemistry. Its ability to participate in alkyne-based reactions, such as cycloadditions, makes it valuable for creating complex molecular architectures efficiently.
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