(R)-3-Aminotetrahydrofuran hydrochloride
97%
- Product Code: 113564
CAS:
1072015-52-1
| Molecular Weight: | 123.58 g./mol | Molecular Formula: | C₄H₁₀ClNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08461720 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, containing both an amine group and a tetrahydrofuran ring, makes it valuable for designing molecules with specific stereochemistry, which is crucial for drug efficacy and safety. It is often employed in the development of antiviral, antibacterial, and central nervous system (CNS) drugs, where precise stereochemical control is required to achieve the desired biological activity. Additionally, it serves as an intermediate in organic synthesis, particularly in the preparation of complex molecules for medicinal chemistry research. Its hydrochloride form enhances stability and solubility, facilitating its use in various chemical reactions and formulations.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £16.96 |
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| 1.000 | 10-20 days | £24.88 |
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| 5.000 | 10-20 days | £79.16 |
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| 10.000 | 10-20 days | £154.02 |
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(R)-3-Aminotetrahydrofuran hydrochloride
This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its structure, containing both an amine group and a tetrahydrofuran ring, makes it valuable for designing molecules with specific stereochemistry, which is crucial for drug efficacy and safety. It is often employed in the development of antiviral, antibacterial, and central nervous system (CNS) drugs, where precise stereochemical control is required to achieve the desired biological activity. Additionally, it serves as an intermediate in organic synthesis, particularly in the preparation of complex molecules for medicinal chemistry research. Its hydrochloride form enhances stability and solubility, facilitating its use in various chemical reactions and formulations.
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| Stable in pH range | - |
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