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Nov . 09, 2024 02:11 Back to list

Exploring the Characteristics and Applications of CAS 9193-49-6 in Various Industries



Exploring CAS 9193-49-6 A Comprehensive Overview


CAS 9193-49-6 refers to a specific chemical compound known as 2-Phenylbenzoic acid. This compound is significant within various scientific and industrial applications due to its unique chemical properties and potential uses. In this article, we will explore the characteristics, applications, synthesis, and safety considerations related to 2-Phenylbenzoic acid.


Chemical Properties

2-Phenylbenzoic acid is an aromatic carboxylic acid, which means it contains a carboxyl group (-COOH) attached to an aromatic ring structure. Its molecular formula is C13H10O2, and it exhibits various functional groups that contribute to its reactivity. The compound typically appears as a white crystalline powder, and its melting point ranges around 130 to 133 degrees Celsius. Its solubility in organic solvents makes it versatile for various applications in organic synthesis.


Applications


One of the primary applications of 2-Phenylbenzoic acid is in the field of organic synthesis, particularly in creating intermediates for pharmaceuticals and agrochemicals. It can serve as a building block for the synthesis of more complex organic compounds, including dyes and pigments. Its unique structure also allows it to function as a photoinitiator in polymerization processes, which is crucial in the manufacturing of plastics and coatings.


Additionally, 2-Phenylbenzoic acid plays a role in the development of ultraviolet (UV) light absorbers, which are essential in formulating products that require protection from UV radiation. This characteristic makes it valuable in cosmetic formulations, adhesives, and various industrial applications where UV stability is a requirement.


china cas 91393-49-6

china cas 91393-49-6

Synthesis


The synthesis of 2-Phenylbenzoic acid can be achieved through several methods. One common route involves the Friedel-Crafts acylation reaction, wherein phenylacetyl chloride reacts with an appropriate aromatic compound in the presence of a Lewis acid catalyst, such as aluminum chloride. This reaction facilitates the attachment of the acyl group to the aromatic ring, leading to the formation of the desired product. Other synthetic pathways may include various condensation reactions or oxidation processes that yield 2-Phenylbenzoic acid from simpler precursors.


Safety Considerations


While 2-Phenylbenzoic acid is utilized in various industries, handling this compound necessitates adherence to appropriate safety protocols. Although it is not classified as highly hazardous, exposure can lead to irritation of the skin and eyes. Therefore, individuals working with this chemical must use personal protective equipment (PPE), including gloves and safety goggles, to minimize exposure risks. Additionally, it is important to work in a well-ventilated area and to follow local regulations regarding chemical handling and disposal.


Conclusion


In summary, CAS 9193-49-6, or 2-Phenylbenzoic acid, is a noteworthy chemical compound with a range of applications attributed to its unique structural properties. From its synthesis pathways to its utilization in pharmaceuticals, materials science, and UV protection, this compound continues to play a vital role in various industrial processes. As research advances, further applications may emerge, highlighting the importance of continued exploration into the potential uses and safe handling of such chemical entities. Understanding the properties and applications of compounds like 2-Phenylbenzoic acid is essential for scientists and industry professionals striving for innovation and safety in chemical utilization.


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