(S)-(Tetrahydrofuran-3-yl)methanamine hydrochloride
97%
- Product Code: 70913
CAS:
1403763-27-8
| Molecular Weight: | 137.61 g./mol | Molecular Formula: | C₅H₁₂ClNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20526350 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its stereochemistry makes it valuable in creating enantiomerically pure compounds, particularly in the development of drugs targeting the central nervous system.
Applied in the production of intermediates for antiviral and antipsychotic medications due to its structural compatibility with bioactive molecules.
Also utilized in organic synthesis for constructing complex molecules, especially in asymmetric synthesis, where its tetrahydrofuran ring and amine functionality provide versatile reactivity.
In medicinal chemistry, it serves as a key precursor for designing molecules with improved pharmacokinetic properties and reduced side effects.
Its hydrochloride form enhances stability and solubility, making it suitable for formulation studies in drug development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £164.88 |
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| 0.250 | 10-20 days | £274.80 |
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| 1.000 | 10-20 days | £661.55 |
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(S)-(Tetrahydrofuran-3-yl)methanamine hydrochloride
Widely used in pharmaceutical research and development as a chiral building block for the synthesis of various active pharmaceutical ingredients (APIs). Its stereochemistry makes it valuable in creating enantiomerically pure compounds, particularly in the development of drugs targeting the central nervous system.
Applied in the production of intermediates for antiviral and antipsychotic medications due to its structural compatibility with bioactive molecules.
Also utilized in organic synthesis for constructing complex molecules, especially in asymmetric synthesis, where its tetrahydrofuran ring and amine functionality provide versatile reactivity.
In medicinal chemistry, it serves as a key precursor for designing molecules with improved pharmacokinetic properties and reduced side effects.
Its hydrochloride form enhances stability and solubility, making it suitable for formulation studies in drug development.
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