1-(2-Nitrovinyl)-4-(trifluoromethyl)benzene

95%

Reagent Code: #219130
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CAS Number 99696-01-2

science Other reagents with same CAS 99696-01-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.14 g/mol
Formula C₉H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD00192359
thermostat Physical Properties
Melting Point 94-96 °C
Boiling Point 254.8±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.355±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both nitrovinyl and trifluoromethyl groups, which are key motifs in bioactive molecules. Its structure allows for further functionalization through reduction of the nitro group or addition across the vinyl bond, making it valuable in medicinal chemistry for building complex organic compounds. Also employed in the development of specialty materials where electron-withdrawing groups influence electronic properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,780.00
inventory 5g
10-20 days ฿34,680.00
inventory 1g
10-20 days ฿11,560.00

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1-(2-Nitrovinyl)-4-(trifluoromethyl)benzene
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Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both nitrovinyl and trifluoromethyl groups, which are key motifs in bioactive molecules. Its structure allows for further functionalization through reduction of the nitro group or addition across the vinyl bond, making it valuable in medicinal chemistry for building complex organic compounds. Also employed in the development of specialty materials where electron-withdrawing groups influence elect
Used as an intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both nitrovinyl and trifluoromethyl groups, which are key motifs in bioactive molecules. Its structure allows for further functionalization through reduction of the nitro group or addition across the vinyl bond, making it valuable in medicinal chemistry for building complex organic compounds. Also employed in the development of specialty materials where electron-withdrawing groups influence electronic properties.
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