1-Iodo-3,5-bis(trifluoromethyl)benzene

98%

  • Product Code: 114900
  Alias:    3,5-bis(trifluoromethyl)iodobenzene 3,5-bis(trifluoromethyl)iodobenzene 1,3-Bistrifluoromethyl-5-iodobenzene
  CAS:    328-73-4
Molecular Weight: 340.01 g./mol Molecular Formula: CF₃₂C₆H₃I
EC Number: MDL Number: MFCD00040837
Melting Point: Boiling Point: 59-61 °C10 mm Hg(lit.)
Density: 1.919 g/mL at 25 °C(lit.) Storage Condition: room temperature, away from light
Product Description: This chemical is primarily used as a building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring iodine and trifluoromethyl groups, makes it a valuable intermediate for cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira reactions, which are essential in creating complex organic molecules. Additionally, it is utilized in the preparation of liquid crystals and advanced materials due to its unique electronic properties. Its trifluoromethyl groups also enhance the lipophilicity and metabolic stability of compounds, making it useful in drug discovery and development.
Product Specification:
Test Specification
Purity (GC) 97-100
Refractive Index N20/D 1.462-1.465
Specific Gravity (20/20) 1.917-1.926
Appearance Colorless To Pink Liquid
Infrared Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿300.00
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-
25.000 10-20 days ฿1,330.00
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-
100.000 10-20 days ฿5,230.00
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1-Iodo-3,5-bis(trifluoromethyl)benzene
This chemical is primarily used as a building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring iodine and trifluoromethyl groups, makes it a valuable intermediate for cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira reactions, which are essential in creating complex organic molecules. Additionally, it is utilized in the preparation of liquid crystals and advanced materials due to its unique electronic properties. Its trifluoromethyl groups also enhance the lipophilicity and metabolic stability of compounds, making it useful in drug discovery and development.
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