N-Methyl-3-(trifluoromethyl)aniline
≥95%
Reagent
Code: #121522
CAS Number
2026-70-2
blur_circular Chemical Specifications
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Molecular Information
Weight
175.15 g/mol
Formula
C₈H₈F₃N
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Registry Numbers
MDL Number
MFCD07368696
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Physical Properties
Boiling Point
195.6°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, protected from light, stored in an inert gas
description Product Description
N-Methyl-3-(trifluoromethyl)aniline is primarily used as an intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a trifluoromethyl group, makes it valuable in the development of drugs with enhanced metabolic stability and bioavailability. It is often employed in the production of agrochemicals, particularly pesticides and herbicides, where the trifluoromethyl group contributes to the efficacy and selectivity of the active ingredients. Additionally, this chemical is utilized in organic synthesis for creating complex molecules in research and industrial applications, particularly in the field of medicinal chemistry. Its role in facilitating the introduction of fluorine atoms into target molecules is crucial for modifying their physical, chemical, and biological properties.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to yellow to brown liquid |
Purity (%) | 94.5-100% |
Infrared Spectrum | Conforms To Structure |
NMR | Conforms To Structure |
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N-Methyl-3-(trifluoromethyl)aniline
N-Methyl-3-(trifluoromethyl)aniline is primarily used as an intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a trifluoromethyl group, makes it valuable in the development of drugs with enhanced metabolic stability and bioavailability. It is often employed in the production of agrochemicals, particularly pesticides and herbicides, where the trifluoromethyl group contributes to the efficacy and selectivity of the active ingredients. Additionally, this chemical is utilized in organic synthesis for creating complex molecules in research and industrial applications, particularly in the field of medicinal chemistry. Its role in facilitating the introduction of fluorine atoms into target molecules is crucial for modifying their physical, chemical, and biological properties.
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