2-(Trifluoromethyl)phenyl isothiocyanate

≥98%

Reagent Code: #77087
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CAS Number 1743-86-8

science Other reagents with same CAS 1743-86-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.18 g/mol
Formula C₈H₄F₃NS
badge Registry Numbers
MDL Number MFCD00039644
thermostat Physical Properties
Boiling Point 220 °C
inventory_2 Storage & Handling
Density 1.3500
Storage room temperature, inert gas

description Product Description

Used in organic synthesis to introduce the trifluoromethylphenyl group into various compounds, enhancing their chemical properties. It is particularly valuable in the development of pharmaceuticals, where it serves as a key intermediate in the production of drugs with improved metabolic stability and bioavailability. Additionally, it is employed in the creation of agrochemicals, contributing to the development of more effective pesticides and herbicides. Its reactivity with amines and other nucleophiles makes it a versatile reagent in the synthesis of heterocyclic compounds, which are important in medicinal chemistry and material science.

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Test Parameter Specification
Appearance Colorless to yellow liquid
Purity 98-100
Proton NMR Spectrum Conforms to Structure
Infrared Spectrum Conforms to Structure
Refractive Index (n20D) 1.563-1.567
Specific Gravity (20°C) 1.348-1.352

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,690.00
inventory 5g
10-20 days ฿6,660.00
inventory 25g
10-20 days ฿20,710.00

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2-(Trifluoromethyl)phenyl isothiocyanate
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Used in organic synthesis to introduce the trifluoromethylphenyl group into various compounds, enhancing their chemical properties. It is particularly valuable in the development of pharmaceuticals, where it serves as a key intermediate in the production of drugs with improved metabolic stability and bioavailability. Additionally, it is employed in the creation of agrochemicals, contributing to the development of more effective pesticides and herbicides. Its reactivity with amines and other nucleophiles

Used in organic synthesis to introduce the trifluoromethylphenyl group into various compounds, enhancing their chemical properties. It is particularly valuable in the development of pharmaceuticals, where it serves as a key intermediate in the production of drugs with improved metabolic stability and bioavailability. Additionally, it is employed in the creation of agrochemicals, contributing to the development of more effective pesticides and herbicides. Its reactivity with amines and other nucleophiles makes it a versatile reagent in the synthesis of heterocyclic compounds, which are important in medicinal chemistry and material science.

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