trans-4-Aminocyclohexanol
98%
- Product Code: 85692
Alias:
Relevant cas number: 6850-65-3 (cis and reverse mixed); 40525-78-8 (cis); trans-aminocyclohexanol; trans-4-amino-1-hydroxycyclohexane
CAS:
27489-62-9
Molecular Weight: | 115.18 g./mol | Molecular Formula: | C₆H₁₃NO |
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EC Number: | MDL Number: | MFCD00067698 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, sealed |
Product Description:
Trans-4-aminocyclohexanol is widely utilized in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting the central nervous system. Its structure serves as a key intermediate in the production of analgesics and anticonvulsants, contributing to the modulation of neurological pathways. Additionally, it plays a role in the creation of chiral building blocks for asymmetric synthesis, enhancing the efficiency of producing enantiomerically pure substances. In material science, it is employed in the preparation of polymers and resins, where its functional groups improve the mechanical and thermal properties of the final products. Its versatility also extends to agrochemical research, aiding in the design of novel pesticides and herbicides with improved efficacy and environmental safety.
Product Specification:
Test | Specification |
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Purity | 98-100 |
MELTING POINT | 108-113 |
APPEARANCE | White to Light yellow to Light orange powder to crystal |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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5.000 | 10-20 days | €7.65 |
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25.000 | 10-20 days | €17.15 |
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100.000 | 10-20 days | €41.68 |
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500.000 | 10-20 days | €176.50 |
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trans-4-Aminocyclohexanol
Trans-4-aminocyclohexanol is widely utilized in the synthesis of pharmaceutical compounds, particularly in the development of drugs targeting the central nervous system. Its structure serves as a key intermediate in the production of analgesics and anticonvulsants, contributing to the modulation of neurological pathways. Additionally, it plays a role in the creation of chiral building blocks for asymmetric synthesis, enhancing the efficiency of producing enantiomerically pure substances. In material science, it is employed in the preparation of polymers and resins, where its functional groups improve the mechanical and thermal properties of the final products. Its versatility also extends to agrochemical research, aiding in the design of novel pesticides and herbicides with improved efficacy and environmental safety.
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