(S)-6-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride

95%

  • Product Code: 38591
  CAS:    1799420-95-3
Molecular Weight: 248.5473 g./mol Molecular Formula: C₉H₁₁BrClN
EC Number: MDL Number: MFCD26585390
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: (S)-6-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride is primarily utilized in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its structure makes it valuable in the development of potential therapeutic agents, particularly in the field of central nervous system (CNS) disorders. Researchers explore its use in creating molecules that may interact with neurotransmitter systems, such as dopamine or serotonin receptors, to address conditions like depression, anxiety, or Parkinson's disease. Additionally, its chiral nature allows for the study of enantiomer-specific effects, which is crucial in optimizing drug efficacy and reducing side effects. This compound also serves as a key intermediate in organic synthesis, enabling the creation of complex molecules for medicinal chemistry and drug discovery projects.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿11,169.00
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(S)-6-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride
(S)-6-Bromo-2,3-dihydro-1H-inden-1-amine hydrochloride is primarily utilized in pharmaceutical research as a chiral building block for the synthesis of biologically active compounds. Its structure makes it valuable in the development of potential therapeutic agents, particularly in the field of central nervous system (CNS) disorders. Researchers explore its use in creating molecules that may interact with neurotransmitter systems, such as dopamine or serotonin receptors, to address conditions like depression, anxiety, or Parkinson's disease. Additionally, its chiral nature allows for the study of enantiomer-specific effects, which is crucial in optimizing drug efficacy and reducing side effects. This compound also serves as a key intermediate in organic synthesis, enabling the creation of complex molecules for medicinal chemistry and drug discovery projects.
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