(3S,4S)-4-Methoxy-N-methylpyrrolidin-3-amine bis(4-methylbenzenesulfonate)

95%

  • Product Code: 36786
  CAS:    372482-03-6
Molecular Weight: 474.59 g./mol Molecular Formula: C₂₀H₃₀N₂O₇S₂
EC Number: MDL Number: MFCD26960917
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its specific structure, featuring a pyrrolidine ring with methoxy and amine functional groups, makes it a valuable building block in the development of drugs targeting the central nervous system. It is often employed in the production of compounds designed to interact with neurotransmitter systems, potentially aiding in the treatment of neurological disorders such as Parkinson's disease, depression, or anxiety. Additionally, its tosylate salt form enhances solubility and stability, making it suitable for formulation processes in drug manufacturing. Researchers also explore its use in creating chiral molecules, leveraging its stereochemistry to achieve enantioselective synthesis in medicinal chemistry.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿3,726.00
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0.250 10-20 days ฿4,788.00
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1.000 10-20 days ฿12,807.00
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(3S,4S)-4-Methoxy-N-methylpyrrolidin-3-amine bis(4-methylbenzenesulfonate)
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its specific structure, featuring a pyrrolidine ring with methoxy and amine functional groups, makes it a valuable building block in the development of drugs targeting the central nervous system. It is often employed in the production of compounds designed to interact with neurotransmitter systems, potentially aiding in the treatment of neurological disorders such as Parkinson's disease, depression, or anxiety. Additionally, its tosylate salt form enhances solubility and stability, making it suitable for formulation processes in drug manufacturing. Researchers also explore its use in creating chiral molecules, leveraging its stereochemistry to achieve enantioselective synthesis in medicinal chemistry.
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