(1R,2R)-2-Aminocyclohexanol
97%
- Product Code: 68242
CAS:
931-16-8
| Molecular Weight: | 115 g./mol | Molecular Formula: | C₆H₁₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08061325 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8℃ |
Product Description:
(1R,2R)-2-Aminocyclohexanol is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the creation of beta-blockers and other cardiovascular medications. Additionally, it is employed in asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. This compound is also explored in the field of organic chemistry for the preparation of complex molecules with specific chiral centers, aiding in the study of stereochemical effects on biological activity.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 96.5 100% |
| appearance | colorles liquid |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿600.00 |
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| 5.000 | 10-20 days | ฿2,120.00 |
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| 25.000 | 10-20 days | ฿8,900.00 |
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(1R,2R)-2-Aminocyclohexanol
(1R,2R)-2-Aminocyclohexanol is primarily utilized in the synthesis of chiral compounds, serving as a key intermediate in the production of pharmaceuticals. Its stereochemistry makes it valuable in the development of enantiomerically pure drugs, particularly in the creation of beta-blockers and other cardiovascular medications. Additionally, it is employed in asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. This compound is also explored in the field of organic chemistry for the preparation of complex molecules with specific chiral centers, aiding in the study of stereochemical effects on biological activity.
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