3-[(Dimethylamino)methyl]-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one

>95%

  • Product Code: 117589
  CAS:    153139-56-1
Molecular Weight: 256.35 g./mol Molecular Formula: C₁₆H₂₀N₂O
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8℃
Product Description: This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structural framework is particularly valuable in the development of compounds targeting the central nervous system, including potential treatments for neurological disorders such as depression, anxiety, and schizophrenia. Additionally, its carbazole core is often explored for its potential anti-inflammatory and anticancer properties, making it a subject of interest in drug discovery and development research. The dimethylamino group further enhances its reactivity, allowing for modifications that can lead to the creation of novel therapeutic agents with improved efficacy and selectivity.
Product Specification:
Test Specification
Appearance White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.025 10-20 days €171.48
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0.050 10-20 days €290.20
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0.100 10-20 days €461.69
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3-[(Dimethylamino)methyl]-9-methyl-1,2,3,9-tetrahydro-4H-carbazol-4-one
This compound is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmacologically active molecules. Its structural framework is particularly valuable in the development of compounds targeting the central nervous system, including potential treatments for neurological disorders such as depression, anxiety, and schizophrenia. Additionally, its carbazole core is often explored for its potential anti-inflammatory and anticancer properties, making it a subject of interest in drug discovery and development research. The dimethylamino group further enhances its reactivity, allowing for modifications that can lead to the creation of novel therapeutic agents with improved efficacy and selectivity.
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