2-Iodobenzotrifluoride

99%

Reagent Code: #117009
label
Alias 2-Iodo-α,α,α-trifluorotoluene;o-trifluoromethyliodobenzene;2-trifluoromethyliodobenzene;2-iodotrifluorobenzene;2-iodotrifluoromethylbenzene;o-iodine Trifluorotoluene
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CAS Number 444-29-1

science Other reagents with same CAS 444-29-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.01 g/mol
Formula C₇H₄F₃I
badge Registry Numbers
EC Number 207-147-1
MDL Number MFCD00001041
thermostat Physical Properties
Boiling Point 197-198 °C750 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.939 g/mL at 25 °C(lit.)
Storage room temperature, away from light

description Product Description

Used primarily as an intermediate in organic synthesis, it plays a crucial role in the production of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the biological activity of compounds, making it valuable in drug development. Additionally, it serves as a building block in the synthesis of complex molecules, particularly in cross-coupling reactions like Suzuki and Sonogashira reactions. In material science, it is employed to modify polymers and create specialty chemicals with unique properties. Its iodine atom allows for further functionalization, enabling the creation of diverse chemical structures.

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Test Parameter Specification
Purity (%) 99%
Refractive Index (20°C) 1.528-1.532
Specific Gravity (20/20°C) 1.92-1.928
Appearance Colorless to Pale Yellow Liquid
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿3,250.00
inventory 500g
10-20 days ฿16,020.00
inventory 5g
10-20 days ฿380.00
inventory 25g
10-20 days ฿880.00

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2-Iodobenzotrifluoride
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Used primarily as an intermediate in organic synthesis, it plays a crucial role in the production of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the biological activity of compounds, making it valuable in drug development. Additionally, it serves as a building block in the synthesis of complex molecules, particularly in cross-coupling reactions like Suzuki and Sonogashira reactions. In material science, it is employed to modify polymers and create specialty chemicals with unique

Used primarily as an intermediate in organic synthesis, it plays a crucial role in the production of pharmaceuticals and agrochemicals. Its trifluoromethyl group enhances the biological activity of compounds, making it valuable in drug development. Additionally, it serves as a building block in the synthesis of complex molecules, particularly in cross-coupling reactions like Suzuki and Sonogashira reactions. In material science, it is employed to modify polymers and create specialty chemicals with unique properties. Its iodine atom allows for further functionalization, enabling the creation of diverse chemical structures.

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