3-Iodobenzotrifluoride

99.5%, with copper shavings as stabilizer

  • Product Code: 118235
  Alias:    3-iodotrifluoromethylbenzene 3-iodotrifluoromethylbenzene m-iodotrifluoromethylbenzene
  CAS:    401-81-0
Molecular Weight: 272.01 g./mol Molecular Formula: C₇H₄F₃I
EC Number: 206-934-7 MDL Number: MFCD00001049
Melting Point: -8 °C Boiling Point: 82-82.5 °C25 mm Hg(lit.)
Density: 1.887 g/mL at 25 °C(lit.) Storage Condition: room temperature, away from light
Product Description: 3-Iodobenzotrifluoride is widely used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the biological activity and metabolic stability of compounds, making it valuable in drug discovery. It is also employed in the synthesis of liquid crystals and advanced materials due to its unique electronic properties. Additionally, it serves as a key building block in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to create complex organic molecules. Its iodine atom allows for further functionalization, enabling the production of diverse chemical structures.
Product Specification:
Test Specification
Refractive Index (20 Degree Celsius) 1.516-1.519
Purity (%) 99.0-100
Specific Gravity (20/20 Degree Celsius) 1.881-1.885
Appearance Colorless To Light Yellow To Light Orange To Yellow To Pink To Red To Brown
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿340.00
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5.000 10-20 days ฿460.00
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50.000 10-20 days ฿1,980.00
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100.000 10-20 days ฿3,860.00
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3-Iodobenzotrifluoride
3-Iodobenzotrifluoride is widely used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the biological activity and metabolic stability of compounds, making it valuable in drug discovery. It is also employed in the synthesis of liquid crystals and advanced materials due to its unique electronic properties. Additionally, it serves as a key building block in cross-coupling reactions, such as Suzuki and Sonogashira couplings, to create complex organic molecules. Its iodine atom allows for further functionalization, enabling the production of diverse chemical structures.
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