10-Methoxy-5H-dibenzo[b,f]azepine-5-carboxamide

97%

  • Product Code: 114978
  CAS:    28721-09-7
Molecular Weight: 266.29 g./mol Molecular Formula: C₁₆H₁₄N₂O₂
EC Number: MDL Number: MFCD08460125
Melting Point: Boiling Point: 468°C at 760 mmHg
Density: 1.31g/cm3 Storage Condition: Room temperature, dry and sealed
Product Description: This compound is primarily utilized in the field of medicinal chemistry and pharmacology due to its structural similarity to tricyclic antidepressants. It is often investigated for its potential therapeutic effects on the central nervous system, particularly in the treatment of mood disorders such as depression and anxiety. Researchers explore its ability to modulate neurotransmitter activity, specifically targeting serotonin and norepinephrine pathways, which are critical in regulating mood and emotional stability. Additionally, its carboxamide group makes it a candidate for further chemical modifications, enabling the development of derivatives with enhanced efficacy or reduced side effects. Its application extends to preclinical studies, where it serves as a key intermediate in synthesizing novel compounds for neurological research.
Product Specification:
Test Specification
Appearance Off-White Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days €38.52
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1.000 10-20 days €78.35
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5.000 10-20 days €233.48
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10-Methoxy-5H-dibenzo[b,f]azepine-5-carboxamide
This compound is primarily utilized in the field of medicinal chemistry and pharmacology due to its structural similarity to tricyclic antidepressants. It is often investigated for its potential therapeutic effects on the central nervous system, particularly in the treatment of mood disorders such as depression and anxiety. Researchers explore its ability to modulate neurotransmitter activity, specifically targeting serotonin and norepinephrine pathways, which are critical in regulating mood and emotional stability. Additionally, its carboxamide group makes it a candidate for further chemical modifications, enabling the development of derivatives with enhanced efficacy or reduced side effects. Its application extends to preclinical studies, where it serves as a key intermediate in synthesizing novel compounds for neurological research.
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