(Z)-7,8-dimethoxy-1H-benzo[d]azepin-2(3H)-one

95%

  • Product Code: 96676
  CAS:    85175-65-1
Molecular Weight: 297.78 g./mol Molecular Formula: C₁₅H₂₀ClNO₃
EC Number: MDL Number: MFCD16875469
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, dry, sealed
Product Description: This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting neurological disorders, as the benzo[d]azepinone core is a common motif in drugs affecting the central nervous system. Researchers leverage its unique chemical framework to design and optimize molecules for potential use as antidepressants, anxiolytics, or antipsychotics. Additionally, its dimethoxy groups offer sites for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. This compound also finds application in academic research, where it serves as a model substrate for studying reaction mechanisms and developing new synthetic methodologies in organic chemistry.
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
0.100 10-20 days €377.26
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0.250 10-20 days €707.04
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(Z)-7,8-dimethoxy-1H-benzo[d]azepin-2(3H)-one
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active molecules. Its structure is particularly valuable in the development of compounds targeting neurological disorders, as the benzo[d]azepinone core is a common motif in drugs affecting the central nervous system. Researchers leverage its unique chemical framework to design and optimize molecules for potential use as antidepressants, anxiolytics, or antipsychotics. Additionally, its dimethoxy groups offer sites for further chemical modifications, enabling the creation of derivatives with enhanced biological activity or improved pharmacokinetic properties. This compound also finds application in academic research, where it serves as a model substrate for studying reaction mechanisms and developing new synthetic methodologies in organic chemistry.
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