(S)-2-Amino-2-cyclohexylethanol
98%
- Product Code: 121199
CAS:
845714-30-9
| Molecular Weight: | 143.23 g./mol | Molecular Formula: | C₈H₁₇NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04112589 | |
| Melting Point: | Boiling Point: | 274°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
(S)-2-Amino-2-cyclohexylethanol is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its structure, featuring both an amino group and a hydroxyl group attached to a cyclohexyl ring, makes it valuable for creating enantiomerically pure compounds. This chemical is often employed in the development of drugs targeting the central nervous system, as its chiral nature can influence the biological activity and selectivity of the final product. Additionally, it serves as an intermediate in the production of agrochemicals, where its stereochemistry can enhance the efficacy of pesticides or herbicides. Its application extends to the field of organic synthesis, where it is utilized to construct complex molecules with specific stereochemical requirements.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $26.91 |
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| 0.250 | 10-20 days | $43.73 |
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| 1.000 | 10-20 days | $108.76 |
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(S)-2-Amino-2-cyclohexylethanol
(S)-2-Amino-2-cyclohexylethanol is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its structure, featuring both an amino group and a hydroxyl group attached to a cyclohexyl ring, makes it valuable for creating enantiomerically pure compounds. This chemical is often employed in the development of drugs targeting the central nervous system, as its chiral nature can influence the biological activity and selectivity of the final product. Additionally, it serves as an intermediate in the production of agrochemicals, where its stereochemistry can enhance the efficacy of pesticides or herbicides. Its application extends to the field of organic synthesis, where it is utilized to construct complex molecules with specific stereochemical requirements.
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