TRANS-2-AMINOCYCLOPENTANOL HYDROCHLORIDE
97%
- Product Code: 58617
CAS:
31775-67-4
Molecular Weight: | 137.61 g./mol | Molecular Formula: | C₅H₁₁NOHCl |
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EC Number: | MDL Number: | MFCD02683551 | |
Melting Point: | 191-196°C (Lit.) | Boiling Point: | |
Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
Trans-2-aminocyclopentanol hydrochloride is primarily utilized in organic synthesis as a chiral building block. Its structure makes it valuable for the preparation of pharmaceuticals, particularly in the development of compounds with specific stereochemistry. It is often employed in the synthesis of bioactive molecules, including drugs targeting neurological disorders or infections. The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is crucial in drug design to ensure efficacy and reduce side effects. Additionally, it serves as an intermediate in the production of fine chemicals and agrochemicals, where precise stereochemical control is required. Its applications also extend to research in asymmetric catalysis and the development of novel synthetic methodologies.
Product Specification:
Test | Specification |
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Purity | 96.5 100% |
Appearance | SOLID |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | $63.31 |
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5.000 | 10-20 days | $207.64 |
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25.000 | 10-20 days | $711.01 |
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TRANS-2-AMINOCYCLOPENTANOL HYDROCHLORIDE
Trans-2-aminocyclopentanol hydrochloride is primarily utilized in organic synthesis as a chiral building block. Its structure makes it valuable for the preparation of pharmaceuticals, particularly in the development of compounds with specific stereochemistry. It is often employed in the synthesis of bioactive molecules, including drugs targeting neurological disorders or infections. The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is crucial in drug design to ensure efficacy and reduce side effects. Additionally, it serves as an intermediate in the production of fine chemicals and agrochemicals, where precise stereochemical control is required. Its applications also extend to research in asymmetric catalysis and the development of novel synthetic methodologies.
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