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4-(Trifluoromethoxy)aniline, also known as 4-TFMA, is an organic compound derived from aniline. It is a colorless liquid with a sweet odor, and is highly soluble in water and organic solvents. 4-TFMA has a wide range of applications in the fields of medicine, chemical synthesis, and environmental protection. It is used...
4-(Trifluoromethoxy)aniline, also known as 4-TFMA, is an organic compound derived from aniline. It is a colorless liquid with a sweet odor, and is highly soluble in water and organic solvents. 4-TFMA has a wide range of applications in the fields of medicine, chemical synthesis, and environmental protection. It is used as a building block for the synthesis of various organic compounds, and as a reagent in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, 4-TFMA is used as an intermediate in the synthesis of various other compounds, such as pharmaceuticals, agrochemicals, and other organic compounds.
A study on the conformational aspects of η6-(4-(trifluoromethoxy)aniline)tricarbonylchromium reveals significant insights. In solid-state, the trifluoromethoxy group is nearly perpendicular to the arene ring, and the amino group is eclipsed by a chromium carbonyl bond. This conformation persists in solution as well (Rose-munch et al., 1994).
4-(Trifluoromethoxy)aniline serves as a precursor for synthesizing important agrochemical intermediates. An improved synthesis process for 2,6-dibromo-4-trifluoromethoxy aniline, derived from 4-trifluoromethoxy aniline, demonstrates high yields and purity, crucial for agrochemical applications (Zhi-yuan, 2011).
Research on 4-trifluoromethyl and 4-trifluoromethoxy derivatives of 4-octyloxy-N-(4-substituted benzylidene) aniline has contributed significantly to liquid crystal technology. These derivatives exhibit stable smectic phases, with the 4-trifluoromethoxy derivative showing a high orientational order in the smectic A phase, highlighting its potential in liquid crystal applications (Miyajima et al., 1995).
In the field of organic materials, 4-(Trifluoromethoxy)aniline plays a role in the synthesis of dendrimers. Its usage in the synthesis and structure of novel G-2 melamine-based dendrimers, incorporating 4-(n-octyloxy)aniline as a peripheral unit, demonstrates its versatility in creating complex organic structures (Morar et al., 2018).
The chemical has been used in synthesizing side-group liquid-crystalline polymers with fluorine-containing mesogens. Its involvement in creating polymers like polyacrylates and polymethacrylates showcases its utility in advanced materials science (Prescher et al., 1995).
Trifluoromethoxy-substituted anilines, including 4-(Trifluoromethoxy)aniline, are critical in organic synthesis, particularly in reactions involving hydrogen/lithium permutation. This property is exploited for structural elaboration in various organic compounds (Leroux et al., 2003).
Product Name : | 4-(Trifluoromethoxy)aniline | ||
CAS No. : | 461-82-5 | Molecular Weight : | 177.12 |
MDL No. : | MFCD00041314 | Purity/ Specification : | |
Molecular Formula : | C7H6F3NO | Storage : | Keep in dark place,Inert atmosphere,Room temperature |
Boiling Point : | - |
GHS Pictogram : | |||
Signal Word : | Danger | Precautionary Statements : | P210-P261-P280-P301+P310-P305+P351+P338 |
UN# : | 2922 | Class : | 8,6.1 |
Hazard Statements : | H227-H301+H311+H331-H315-H318-H373 | Packing Group : | Ⅲ |