4-Aminocyclohexaneethanol
≥98%, cis-trans mixture
- Product Code: 119048
CAS:
857831-26-6
| Molecular Weight: | 143.23 g./mol | Molecular Formula: | C₈H₁₇NO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 85°C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
4-Aminocyclohexaneethanol is primarily utilized in the pharmaceutical and chemical industries as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring both an amino group and a hydroxyl group, makes it a versatile building block for the development of drugs, particularly those targeting the central nervous system. It is often employed in the production of analgesics, antidepressants, and other therapeutic agents that require cyclohexane-based frameworks. Additionally, it serves as a precursor in the creation of specialty chemicals, including polymers and surfactants, where its functional groups enable further chemical modifications. Its role in organic synthesis also extends to the development of chiral compounds, contributing to advancements in asymmetric synthesis and catalysis.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Almost White Powder To Lump |
| Purity (%) | 98-100 |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | ฿2,360.00 |
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| 1.000 | 10-20 days | ฿8,500.00 |
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4-Aminocyclohexaneethanol
4-Aminocyclohexaneethanol is primarily utilized in the pharmaceutical and chemical industries as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring both an amino group and a hydroxyl group, makes it a versatile building block for the development of drugs, particularly those targeting the central nervous system. It is often employed in the production of analgesics, antidepressants, and other therapeutic agents that require cyclohexane-based frameworks. Additionally, it serves as a precursor in the creation of specialty chemicals, including polymers and surfactants, where its functional groups enable further chemical modifications. Its role in organic synthesis also extends to the development of chiral compounds, contributing to advancements in asymmetric synthesis and catalysis.
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