3-Iodobenzotrifluoride

98%, with copper shavings as stabilizer

  • Product Code: 118231
  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 in organic synthesis as a versatile building block, particularly in cross-coupling reactions such as the Suzuki and Heck reactions. Its iodine atom serves as a reactive site for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of liquid crystals and other specialty chemicals due to its trifluoromethyl group, which enhances stability and reactivity. Its applications also extend to the development of organic electronic materials and catalysts in various industrial processes.
Product Specification:
Test Specification
Refractive Index (20 Degree Celsius) 1.516-1.519
Assay (GC) 98-100
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
2.000 10-20 days ฿320.00
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10.000 10-20 days ฿450.00
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25.000 10-20 days ฿750.00
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50.000 10-20 days ฿1,460.00
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250.000 10-20 days ฿6,880.00
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3-Iodobenzotrifluoride
3-Iodobenzotrifluoride is widely used in organic synthesis as a versatile building block, particularly in cross-coupling reactions such as the Suzuki and Heck reactions. Its iodine atom serves as a reactive site for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of liquid crystals and other specialty chemicals due to its trifluoromethyl group, which enhances stability and reactivity. Its applications also extend to the development of organic electronic materials and catalysts in various industrial processes.
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