(1R,2R,5R)-()-2-Hydroxy-3-pinanone
99%
- Product Code: 70849
Alias:
(1R,2R,5R)-2-Hydroxy-2,6,6-trimethyl-bicyclo[3.1.1]heptan-3-one
(1R,2R,5R)-(+)-2-Hydroxy-3-pinanone
CAS:
24047-72-1
| Molecular Weight: | 168.24 g./mol | Molecular Formula: | C₁₀H₁₆O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00191522 | |
| Melting Point: | 37-39 °C(lit.) | Boiling Point: | 245 °C(lit.) |
| Density: | 1.059 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
This compound is primarily utilized in the synthesis of chiral molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its unique structure allows it to serve as a building block in asymmetric synthesis, particularly in the creation of complex organic molecules with specific stereochemistry. Additionally, it is employed in the development of fragrances and flavoring agents due to its distinct aromatic properties. In research, it acts as a key intermediate in studying chemical reactions and developing new synthetic pathways.
Product Specification:
| Test | Specification |
|---|---|
| PurityGC | 99 100% |
| SPECIFIC ROTATION A20DC0.5 CHCL3 | 30-34 |
| APPEARANCE | COLORLESS OR OFF-WHITE SOLID OR LIQUID |
| INFRARED SPECTRUM | Conforms to Structure |
| NOTE: | This product is low melting point solid,may change state in different environments (solid, liquid or semi-solid) |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | €64.58 |
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| 5.000 | 10-20 days | €200.64 |
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(1R,2R,5R)-()-2-Hydroxy-3-pinanone
This compound is primarily utilized in the synthesis of chiral molecules, making it valuable in the production of pharmaceuticals and fine chemicals. Its unique structure allows it to serve as a building block in asymmetric synthesis, particularly in the creation of complex organic molecules with specific stereochemistry. Additionally, it is employed in the development of fragrances and flavoring agents due to its distinct aromatic properties. In research, it acts as a key intermediate in studying chemical reactions and developing new synthetic pathways.
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