(R)-(-)-Tetrahydrofurfurylamine
99%
- Product Code: 71673
Alias:
(R)-2-Aminomethyltetrahydrofuran
CAS:
7202-43-9
| Molecular Weight: | 101.15 g./mol | Molecular Formula: | C₅H₁₁NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00192476 | |
| Melting Point: | Boiling Point: | 55 °C18 mm Hg(lit.) | |
| Density: | 0.98 g/mL at 25 °C(lit.) | Storage Condition: | room temperature, flammable area |
Product Description:
This chemical is widely used as a chiral building block in the synthesis of various pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry for efficacy. It serves as a key intermediate in the development of drugs targeting the central nervous system, including antidepressants and anti-anxiety medications, due to its ability to influence neurotransmitter activity. Additionally, it is employed in the creation of agrochemicals, such as herbicides and fungicides, where its stereochemistry enhances the selectivity and potency of the final product. In organic synthesis, it is utilized as a precursor for the preparation of complex molecules, including natural products and fine chemicals, where its chiral nature is crucial for achieving desired biological activity. Its versatility also extends to the field of asymmetric catalysis, where it acts as a ligand or catalyst in enantioselective reactions, enabling the production of optically pure compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to yellow liquid |
| PURITY | 99-100 |
| REFRACTURE INDEX N20D | 1.453-1.457 |
| SPECIFIC ROTATION A20DC4MEOH | -18 -12 |
| INFRARED SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft11,636.04 |
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| 1.000 | 10-20 days | Ft22,625.63 |
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| 5.000 | 10-20 days | Ft91,795.40 |
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(R)-(-)-Tetrahydrofurfurylamine
This chemical is widely used as a chiral building block in the synthesis of various pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry for efficacy. It serves as a key intermediate in the development of drugs targeting the central nervous system, including antidepressants and anti-anxiety medications, due to its ability to influence neurotransmitter activity. Additionally, it is employed in the creation of agrochemicals, such as herbicides and fungicides, where its stereochemistry enhances the selectivity and potency of the final product. In organic synthesis, it is utilized as a precursor for the preparation of complex molecules, including natural products and fine chemicals, where its chiral nature is crucial for achieving desired biological activity. Its versatility also extends to the field of asymmetric catalysis, where it acts as a ligand or catalyst in enantioselective reactions, enabling the production of optically pure compounds.
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