(1R)-1-(5-Methyl-2-furyl)-1-propanamine, D-Tartaric acid
>95%
- Product Code: 78440
Alias:
Related CAS number: 779340-48-6
CAS:
780760-09-0
Molecular Weight: | 289.3 g./mol | Molecular Formula: | C₁₂H₁₉NO₇ |
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EC Number: | MDL Number: | ||
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 or intermediate in the synthesis of more complex molecules. Its chiral nature makes it valuable for producing enantiomerically pure drugs, which can enhance efficacy and reduce side effects. It is often employed in the development of active pharmaceutical ingredients (APIs) for treating neurological or psychiatric disorders, where stereochemistry plays a critical role in drug activity. Additionally, its tartaric acid component aids in improving solubility and stability of the final drug product. The compound may also find use in research settings for studying stereochemical interactions and developing novel therapeutic agents.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | White Solid |
PURITY | 95-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
---|---|---|---|
0.250 | 10-20 days | ฿38,880.00 |
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(1R)-1-(5-Methyl-2-furyl)-1-propanamine, D-Tartaric acid
This compound is primarily utilized in the pharmaceutical industry as a chiral building block or intermediate in the synthesis of more complex molecules. Its chiral nature makes it valuable for producing enantiomerically pure drugs, which can enhance efficacy and reduce side effects. It is often employed in the development of active pharmaceutical ingredients (APIs) for treating neurological or psychiatric disorders, where stereochemistry plays a critical role in drug activity. Additionally, its tartaric acid component aids in improving solubility and stability of the final drug product. The compound may also find use in research settings for studying stereochemical interactions and developing novel therapeutic agents.
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