(R)-1-(pyridin-3-yl)ethanamine hydrochloride
98%
- Product Code: 70265
CAS:
1169576-97-9
Molecular Weight: | 158.63 g./mol | Molecular Formula: | C₇H₁₁ClN₂ |
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EC Number: | MDL Number: | MFCD12068450 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
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, featuring a pyridine ring and an amine group, makes it valuable in the development of drugs targeting the central nervous system, particularly for conditions like depression, anxiety, and neurodegenerative diseases. It is also employed in the creation of ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. Additionally, its hydrochloride form ensures improved solubility and stability, making it suitable for formulation in drug delivery systems. Researchers also explore its potential in designing novel compounds for medicinal chemistry studies, particularly in optimizing pharmacokinetic properties.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿3,141.00 |
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0.250 | 10-20 days | ฿12,591.00 |
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(R)-1-(pyridin-3-yl)ethanamine 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, featuring a pyridine ring and an amine group, makes it valuable in the development of drugs targeting the central nervous system, particularly for conditions like depression, anxiety, and neurodegenerative diseases. It is also employed in the creation of ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions. Additionally, its hydrochloride form ensures improved solubility and stability, making it suitable for formulation in drug delivery systems. Researchers also explore its potential in designing novel compounds for medicinal chemistry studies, particularly in optimizing pharmacokinetic properties.
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