1-(4-bromo-3-methylphenyl)ethanamine hydrochloride

95%

  • Product Code: 150817
  CAS:    117520-24-8
Molecular Weight: 250.56 g./mol Molecular Formula: C₉H₁₃BrClN
EC Number: MDL Number: MFCD31706598
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, inert atmosphere
Product Description: Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active agents. Its structural features allow for effective modification to produce bioactive molecules with improved binding affinity and metabolic stability. Commonly employed in research settings for the preparation of analogs in medicinal chemistry programs targeting neurological disorders such as depression, anxiety, and obsessive-compulsive disorder. Also utilized in the production of radiolabeled derivatives for receptor binding studies. Its hydrochloride salt form enhances solubility and handling in aqueous reaction media, making it suitable for coupling reactions and multistep syntheses in drug discovery.
Sizes / Availability / Pricing:
Size Availability Price Quantity
0.100 10-20 days $505.19
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0.250 10-20 days $758.38
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1.000 10-20 days $1,898.72
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1-(4-bromo-3-methylphenyl)ethanamine hydrochloride
Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active agents. Its structural features allow for effective modification to produce bioactive molecules with improved binding affinity and metabolic stability. Commonly employed in research settings for the preparation of analogs in medicinal chemistry programs targeting neurological disorders such as depression, anxiety, and obsessive-compulsive disorder. Also utilized in the production of radiolabeled derivatives for receptor binding studies. Its hydrochloride salt form enhances solubility and handling in aqueous reaction media, making it suitable for coupling reactions and multistep syntheses in drug discovery.
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