4-Nitrochalcone

≥95%

  • Product Code: 119526
  CAS:    1222-98-6
Molecular Weight: 253.26 g./mol Molecular Formula: C₁₅H₁₁NO₃
EC Number: MDL Number: MFCD00007382
Melting Point: 163-167°C Boiling Point:
Density: Storage Condition: room temperature
Product Description: 4-Nitrochalcone is primarily used in research and development within the field of organic chemistry. It serves as a key intermediate in the synthesis of various complex molecules, particularly in the study of chalcone derivatives. These derivatives are often explored for their potential biological activities, including anti-inflammatory, anticancer, and antimicrobial properties. Additionally, 4-Nitrochalcone is utilized in photochemical studies due to its ability to undergo photoisomerization, making it valuable in understanding light-induced molecular transformations. Its nitro group also makes it a useful compound in the development of new materials and sensors, where nitroaromatic compounds are often employed for their electron-withdrawing characteristics.
Product Specification:
Test Specification
Appearance Slightly Pale Yellow To Yellow Crystal Or Powder
Purity (%) 95-100
Melting Point (Degree Celsius) 163.0-167.0
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿770.00
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5.000 10-20 days ฿2,280.00
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4-Nitrochalcone
4-Nitrochalcone is primarily used in research and development within the field of organic chemistry. It serves as a key intermediate in the synthesis of various complex molecules, particularly in the study of chalcone derivatives. These derivatives are often explored for their potential biological activities, including anti-inflammatory, anticancer, and antimicrobial properties. Additionally, 4-Nitrochalcone is utilized in photochemical studies due to its ability to undergo photoisomerization, making it valuable in understanding light-induced molecular transformations. Its nitro group also makes it a useful compound in the development of new materials and sensors, where nitroaromatic compounds are often employed for their electron-withdrawing characteristics.
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