(S)-7-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride

97%

  • Product Code: 113836
  CAS:    2061996-47-0
Molecular Weight: 187.64 g./mol Molecular Formula: C₁₀H₁₈O₄
EC Number: MDL Number: MFCD30609561
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, dry and sealed
Product Description: (S)-7-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its structural properties make it a valuable building block for developing molecules that interact with specific receptors in the brain, such as serotonin or dopamine receptors. This compound is often explored for its potential in creating drugs aimed at treating conditions like depression, anxiety, and other mental health disorders. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, which can enhance efficacy and reduce side effects. Researchers also investigate its use in designing novel therapeutic agents for neurodegenerative diseases, leveraging its unique chemical framework to improve drug specificity and potency.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days €243.14
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0.250 10-20 days €485.80
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(S)-7-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride
(S)-7-Fluoro-2,3-dihydro-1H-inden-1-amine hydrochloride is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various bioactive compounds, particularly those targeting neurological disorders. Its structural properties make it a valuable building block for developing molecules that interact with specific receptors in the brain, such as serotonin or dopamine receptors. This compound is often explored for its potential in creating drugs aimed at treating conditions like depression, anxiety, and other mental health disorders. Additionally, its chiral nature allows for the development of enantiomerically pure drugs, which can enhance efficacy and reduce side effects. Researchers also investigate its use in designing novel therapeutic agents for neurodegenerative diseases, leveraging its unique chemical framework to improve drug specificity and potency.
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