3-Nitrochalcone

≥98%

  • Product Code: 118205
  CAS:    614-48-2
Molecular Weight: 253.26 g./mol Molecular Formula: C₁₅H₁₁NO₃
EC Number: MDL Number: MFCD00024571
Melting Point: 142-146°C Boiling Point:
Density: Storage Condition: room temperature
Product Description: 3-Nitrochalcone is primarily utilized in organic synthesis and research due to its unique chemical structure, which makes it a valuable intermediate in the preparation of various heterocyclic compounds. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential anti-inflammatory, anticancer, and antimicrobial properties. Additionally, its nitro group makes it a useful precursor in the study of nitro-reduction reactions, which are important in drug metabolism and environmental chemistry. In material science, 3-Nitrochalcone is explored for its potential in creating organic electronic materials and light-sensitive compounds. Its application in photochemical studies is also notable, as it can be used to investigate photo-induced reactions and molecular interactions.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.200 10-20 days $48.22
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1.000 10-20 days $142.78
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3-Nitrochalcone
3-Nitrochalcone is primarily utilized in organic synthesis and research due to its unique chemical structure, which makes it a valuable intermediate in the preparation of various heterocyclic compounds. It is often employed in the development of pharmaceuticals, particularly in the synthesis of compounds with potential anti-inflammatory, anticancer, and antimicrobial properties. Additionally, its nitro group makes it a useful precursor in the study of nitro-reduction reactions, which are important in drug metabolism and environmental chemistry. In material science, 3-Nitrochalcone is explored for its potential in creating organic electronic materials and light-sensitive compounds. Its application in photochemical studies is also notable, as it can be used to investigate photo-induced reactions and molecular interactions.
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