2-Iodo-1-nitro-4-(trifluoromethyl)benzene

95%

Reagent Code: #198569
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CAS Number 16499-53-9

science Other reagents with same CAS 16499-53-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317 g/mol
Formula C₇H₃F₃INO₂
thermostat Physical Properties
Boiling Point 286.6±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.020±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry, light-proof

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in multi-step reactions, particularly in the development of fluorinated organic compounds. The iodo and nitro groups serve as reactive sites for cross-coupling reactions and nucleophilic substitutions, making it valuable in constructing complex molecules. Commonly employed in the preparation of bioactive agents where the trifluoromethyl group enhances metabolic stability and lipophilicity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,650.00
inventory 1g
10-20 days ฿15,200.00
inventory 5g
10-20 days ฿53,130.00

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2-Iodo-1-nitro-4-(trifluoromethyl)benzene
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in multi-step reactions, particularly in the development of fluorinated organic compounds. The iodo and nitro groups serve as reactive sites for cross-coupling reactions and nucleophilic substitutions, making it valuable in constructing complex molecules. Commonly employed in the preparation of bioactive agents where the trifluoromethyl group enhances metabolic sta

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for selective functionalization in multi-step reactions, particularly in the development of fluorinated organic compounds. The iodo and nitro groups serve as reactive sites for cross-coupling reactions and nucleophilic substitutions, making it valuable in constructing complex molecules. Commonly employed in the preparation of bioactive agents where the trifluoromethyl group enhances metabolic stability and lipophilicity.

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