2<\/a>49-91-2 consists of a benzoyl group attached to a four-membered azetidinone ring, which is further substituted with a phenyl group and a triethylsilyl oxygen. This arrangement results in a polar compound with a molecular weight of 284.36 g\/mol. The presence of the benzoyl group and the triethylsilyl oxygen imparts specific properties to the compound, such as solubility in organic solvents and reactivity towards nucleophiles.<\/p>\nSynthesis of CAS 149249-91-2<\/h3>\n
The synthesis of CAS 149249-91-2 involves several steps, including the formation of the azetidinone ring and the subsequent substitution with the benzoyl and phenyl groups. One common synthetic route starts with the reaction of a \u03b2-ketoester with a triethylsilylating agent, followed by cyclization to form the azetidinone ring. Subsequent steps involve the introduction of the benzoyl and phenyl groups through nucleophilic acyl substitution reactions.<\/p>\n
Applications of CAS 149249-91-2<\/h3>\n
CAS 149249-91-2 has several potential applications due to its unique structure and properties. In the pharmaceutical industry, it may serve as a precursor for the synthesis of bioactive compounds with various therapeutic applications. Additionally, its reactivity towards nucleophiles makes it a valuable intermediate in the synthesis of agrochemicals and materials with specific functionalities.<\/p>\n
Significance in Modern Chemistry<\/h3>\n
The study of CAS 149249-91-2 contributes to the broader field of organic chemistry by providing insights into the synthesis and reactivity of azetidinones. It also highlights the importance of understanding the structure-activity relationships of organic compounds, which is crucial for the development of new drugs and materials. Furthermore, the exploration of this compound's potential applications underscores the significance of interdisciplinary research in modern chemistry.<\/p>\n
Consideraciones medioambientales y sanitarias<\/h3>\n
As with any chemical compound, the environmental and health considerations of CAS 149249-91-2 are of paramount importance. It is essential to assess the compound's toxicity, environmental persistence, and potential for bioaccumulation. Proper handling, storage, and disposal practices must be followed to minimize any potential risks associated with its use.<\/p>\n
Conclusi\u00f3n<\/h3>\n
In conclusion, CAS 149249-91-2: (3R,4S)-1-Benzoyl-4-Phenyl-3-(Triethylsilyl)oxy-2-Azetidinone is a complex organic compound with a wide range of potential applications. Its unique structure and properties make it a valuable subject of study in organic chemistry. By unlocking the secrets of this compound, researchers can gain a deeper understanding of its synthesis, reactivity, and potential uses in various fields. This knowledge not only contributes to the advancement of chemistry but also opens doors for the development of new drugs, agrochemicals, and materials with improved functionalities.<\/p>\n
Keywords: CAS 149249-91-2, (3R,4S)-1-Benzoyl-4-Phenyl-3-(Triethylsilyl)oxy-2-Azetidinone, azetidinones, synthesis, properties, applications, organic chemistry<\/p>","protected":false},"excerpt":{"rendered":"
AbstractThis article delves into the chemical compound CAS 149249-91-2, identified as (3R,4S)-1-Benzoyl-4-Phenyl-3-(Triethylsilyl)oxy-2-Azet<\/p>","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1],"tags":[187,2596],"class_list":["post-25518","post","type-post","status-publish","format-standard","hentry","category-uncategorized","tag-cas","tag-secrets"],"_links":{"self":[{"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/posts\/25518","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/comments?post=25518"}],"version-history":[{"count":2,"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/posts\/25518\/revisions"}],"predecessor-version":[{"id":27921,"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/posts\/25518\/revisions\/27921"}],"wp:attachment":[{"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/media?parent=25518"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/categories?post=25518"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/chemneo.com\/es\/wp-json\/wp\/v2\/tags?post=25518"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}