{"id":25796,"date":"2024-12-04T22:22:21","date_gmt":"2024-12-04T14:22:21","guid":{"rendered":"https:\/\/chemneo.com\/?p=25796"},"modified":"2024-12-04T14:49:19","modified_gmt":"2024-12-04T06:49:19","slug":"discover-the-power-of-2-aminobenzotrifluoride-cas-88-17-5%ef%bc%9a-everything-you-need-to-know","status":"publish","type":"post","link":"https:\/\/chemneo.com\/en\/25796","title":{"rendered":"Discover the Power of 2-Aminobenzotrifluoride (CAS 88-17-5)\uff1a Everything You Need to Know"},"content":{"rendered":"<h3>Abstract<\/h3>\n<p>This article provides an in-depth exploration of 2-Aminobenzotrifluoride (CAS 88-17-5), a versatile organic compound with significant applications in various fields. From its chemical properties and synthesis methods to its uses in pharmaceuticals, materials science, and organic synthesis, this article aims to cover everything you need to know about this compound. By understanding its potential and limitations, researchers and industry professionals can make informed decisions regarding its utilization.<\/p>\n<h3>Introduction to 2-Aminobenzotrifluoride (CAS 88-17-5)<\/h3>\n<p>2-Aminobenzotrifluoride, also known as 2-trifluoromethylbenzenamine, is an organic compound with the chemical formula C<sub>7<\/sub>H<sub>6<\/sub>F<sub>3<\/sub>N. It is a white crystalline solid that is highly flammable and should be handled with care. This compound is widely used in the synthesis of pharmaceuticals, agrochemicals, and materials. Its unique properties make it a valuable building block in organic chemistry.<\/p>\n<h3>Chemical Properties of 2-Aminobenzotrifluoride<\/h3>\n<p>2-Aminobenzotrifluoride is characterized by its trifluoromethyl group, which imparts it with a high degree of electron-withdrawing ability. This property makes it a valuable intermediate in the synthesis of various organic compounds. The compound is also known for its high reactivity, which allows it to participate in various chemical reactions, including nucleophilic substitution, electrophilic aromatic substitution, and reduction reactions.<\/p>\n<h3>Synthesis of 2-Aminobenzotrifluoride<\/h3>\n<p>The synthesis of 2-Aminobenzotrifluoride can be achieved through several methods, including the reaction of 2-trifluoromethylbenzaldehyde with an amine, or the reaction of 2-trifluoromethylbenzonitrile with a reducing agent. These methods involve the use of specific reagents and conditions that ensure the formation of the desired product with high purity. The choice of synthesis method depends on the scale of production and the desired purity of the compound.<\/p>\n<h3>Applications in Pharmaceuticals<\/h3>\n<p>2-Aminobenzotrifluoride plays a crucial role in the synthesis of various pharmaceuticals. Its trifluoromethyl group can be used to introduce specific functional groups into drug molecules, enhancing their efficacy and selectivity. This compound is used in the synthesis of antiviral agents, anti-inflammatory drugs, and cancer therapeutics. Its versatility makes it a valuable tool in drug discovery and development.<\/p>\n<h3>Applications in Materials Science<\/h3>\n<p>In materials science, 2-Aminobenzotrifluoride is used as a building block for the synthesis of novel materials with unique properties. For instance, it can be used to create polymeric materials with improved thermal stability and flame retardancy. Additionally, its reactivity allows for the development of new organic-inorganic hybrid materials with enhanced mechanical and electrical properties.<\/p>\n<h3>Applications in Organic Synthesis<\/h3>\n<p>Organic chemists utilize 2-Aminobenzotrifluoride as a key intermediate in the synthesis of complex organic molecules. Its ability to undergo various chemical transformations makes it a valuable tool in the construction of carbon frameworks. This compound is particularly useful in the synthesis of heterocyclic compounds, natural products, and bioactive molecules.<\/p>\n<h3>Environmental and Health Considerations<\/h3>\n<p>While 2-Aminobenzotrifluoride offers numerous benefits, it is important to consider its environmental and health implications. The compound is classified as a hazardous substance due to its potential to cause harm to humans and the environment. Proper handling, storage, and disposal procedures are essential to minimize risks. Researchers and industry professionals should adhere to safety guidelines to ensure the safe use of this compound.<\/p>\n<h3>Conclusion<\/h3>\n<p>In conclusion, 2-Aminobenzotrifluoride (CAS 88-17-5) is a versatile organic compound with significant applications in pharmaceuticals, materials science, and organic synthesis. Its unique chemical properties and reactivity make it a valuable tool in the development of new materials and drugs. However, it is crucial to handle this compound with care due to its potential hazards. By understanding its properties, synthesis methods, and applications, researchers and industry professionals can make informed decisions regarding its utilization.<\/p>\n<p>Keywords: 2-Aminobenzotrifluoride, CAS 88-17-5, organic synthesis, pharmaceuticals, materials science, environmental health considerations.<\/p>","protected":false},"excerpt":{"rendered":"<p>AbstractThis article provides an in-depth exploration of 2-Aminobenzotrifluoride (CAS 88-17-5), a versatil<\/p>","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[2770,187],"class_list":["post-25796","post","type-post","status-publish","format-standard","hentry","category-uncategorized","tag-aminobenzotrifluoride","tag-cas"],"_links":{"self":[{"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/posts\/25796","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/comments?post=25796"}],"version-history":[{"count":1,"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/posts\/25796\/revisions"}],"predecessor-version":[{"id":25797,"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/posts\/25796\/revisions\/25797"}],"wp:attachment":[{"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/media?parent=25796"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/categories?post=25796"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/chemneo.com\/en\/wp-json\/wp\/v2\/tags?post=25796"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}