Why is 185112-61-2 Better?

Why is 185112-61-2 Better? In the world of chemistry, understanding the minute details of compounds can make a significant difference in research outcomes and practical applications. One such compound, known by its CAS number 185112-61-2, also referred to in various contexts as 3-bromophenyl carbazole, has been making waves in the scientific community for its unique properties and versatile applications. Below, we explore why this compound is superior in its category. Applications and Benefits of 185112-61-2 Synthesis of Key Intermediates The compound 185112-61-2 plays a pivotal role as an intermediate in the synthesis of various chemical compounds. It exhibits high reactivity and stability which are critical in creating complex molecules. This compound’s ability to form a strong foundation compound for advanced synthesis is seen in its usage in key laboratory preparations. Example 12: Synthesis of Compound 80 With sodium t-butanolate;1,1'-bis(diphenylphosphino)ferrocene; tris-(dibenzylideneacetone)dipalladium(0); In xylene; for 24h;Inert atmosphere; Reflux; Example 12; Synthesis of Compound 80 Step 1. Carbazole (7.3 g, 43.7 mmol), 3-bromoiodobenzene (25 g, 87.3 mmol) and sodium t-buthoxide (8.4 g, 87.3 mmol) is suspended in 150 mL of dry xylene under nitrogen atmosphere. Tris(dibenzylideneacetone)dipalladium (200 mg) and 1,1'-bis(diphenylphosphino) ferrocene (400 mg) are added as one portion and the reaction is heated to reflux and stirred under nitrogen atmosphere for 24 h. After cooling the xylene is evaporated and the residue is subjected to column chromatography on silica gel, providing 3-bromophenyl carbazole (9.5 g, yellow solidified oil). Efficiency in Industrial Applications The practical efficiency of 185112-61-2 in industrial applications cannot be overstated. This compound is used in the synthesis and production of various industrial chemicals. Its reactivity rates and yields make it an irreplaceable component in certain manufacturing processes. Preparation Example 1 With potassium carbonate; In 1,2-dichloro-benzene; Preparation Example 1 Synthesis of Intermediate 4 g of carbazole, 8.08 g of 1-bromo-3-iodobenzene, 13.2 g of potassium carbonate, 3.08 g of copper powder and 0.63 g of dibenzo-18-crown-6 were dissolved in 30 mL of o-dichlorobenzene, and the resulting solution was refluxed at a steady 100°C. After completion of the reaction, the reaction mixture was extracted with dichloromethane and distilled water, and the solvent was dried. The resulting solid was filtered and purified, yielding 9-(3-bromophenyl)-9H-carbazole as an intermediate. Environmental Impact and Sustainability Another significant advantage of using 185112-61-2 is its relatively low environmental impact due to its efficiency and the minimal by-products produced during its reactions. This characteristic makes it an ideal candidate for green chemistry initiatives, where reducing waste and improving sustainability are paramount. High Yield and Purity When synthesized correctly, 185112-61-2 yields high-purity products. Its synthesis pathways, when compared to other similar compounds, often result in higher yields and fewer impurities, ensuring that end-use applications receive only the best quality materials. This is evident in the various reactions where it is used as a critical intermediate. Contact us to discuss your requirements of palladium bromide, palladium diacetate supplier. Conclusion In conclusion, the compound known as 185112-61-2 is superior for a plethora of reasons ranging from its reactivity and efficiency in synthesis to its low environmental impact and high yield purity. For any industry or research environment looking to leverage a high-quality compound for advanced processes, this compound stands out as the go-to choice. For further details about obtaining this compound or discussing its applications, click on 185112-61-2 for more information.