3-Iodobenzotrifluoride
99.5%, with copper shavings as stabilizer
Reagent
Code: #118235
Alias
3-iodotrifluoromethylbenzene 3-iodotrifluoromethylbenzene m-iodotrifluoromethylbenzene
CAS Number
401-81-0
blur_circular Chemical Specifications
scatter_plot
Molecular Information
Weight
272.01 g/mol
Formula
C₇H₄F₃I
badge
Registry Numbers
EC Number
206-934-7
MDL Number
MFCD00001049
thermostat
Physical Properties
Melting Point
-8 °C
Boiling Point
82-82.5 °C25 mm Hg(lit.)
inventory_2
Storage & Handling
Density
1.887 g/mL at 25 °C(lit.)
Storage
room temperature, away from light
description 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.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Refractive Index (20°C) | 1.516-1.519 |
Purity (%) | 99.0-100 |
Specific Gravity (20/20°C) | 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 |
shopping_cart Available Sizes & Pricing
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.
Mechanism | - |
Appearance | - |
Longevity | - |
Strength | - |
Storage | - |
Shelf Life | - |
Allergen(s) | - |
Dosage (Range) | - |
Recommended Dosage | - |
Dosage (Per Day) | - |
Recommended Dosage (Per Day) | - |
Mix Method | - |
Heat Resistance | - |
Stable in pH range | - |
Solubility | - |
Product Types | - |
INCI | - |
Purchase History for
Loading purchase history...
Cart
No products
Subtotal:
฿0.00
Total
฿0.00
THB