2-Chloro-5-(trifluoromethyl)phenyl Isocyanate

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Reagent Code: #160831
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CAS Number 50528-86-4

science Other reagents with same CAS 50528-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.56 g/mol
Formula C₈H₃ClF₃NO
badge Registry Numbers
MDL Number MFCD00037029
thermostat Physical Properties
Boiling Point 64 °C/0.7kPa
inventory_2 Storage & Handling
Density 1.46g/mL
Storage  2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound plays a key role in forming urea and carbamate derivatives that exhibit biological activity. Its electrophilic isocyanate group readily reacts with amines and alcohols, making it valuable in constructing complex molecules for crop protection agents, particularly insecticides and herbicides. It is also employed in the development of specialty polymers and functional materials where fluorinated aromatic segments enhance stability and performance. Due to its reactivity and lachrymatory nature, it is handled under controlled conditions in industrial and laboratory settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿910.00
inventory 1g
10-20 days ฿1,980.00
inventory 5g
10-20 days ฿8,500.00
inventory 25g
10-20 days ฿38,000.00

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2-Chloro-5-(trifluoromethyl)phenyl Isocyanate
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Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound plays a key role in forming urea and carbamate derivatives that exhibit biological activity. Its electrophilic isocyanate group readily reacts with amines and alcohols, making it valuable in constructing complex molecules for crop protection agents, particularly insecticides and herbicides. It is also employed in the development of specialty polymers and functional materials where fluorinated aromatic s

Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals, this compound plays a key role in forming urea and carbamate derivatives that exhibit biological activity. Its electrophilic isocyanate group readily reacts with amines and alcohols, making it valuable in constructing complex molecules for crop protection agents, particularly insecticides and herbicides. It is also employed in the development of specialty polymers and functional materials where fluorinated aromatic segments enhance stability and performance. Due to its reactivity and lachrymatory nature, it is handled under controlled conditions in industrial and laboratory settings.

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