77771-05-2 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-fluoro-3-phenoxyphenyl)-1,3-dioxolane is utilized as a building block for the synthesis of complex molecules in drug development. Its unique structure and properties contribute to the creation of new pharmaceutical agents with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(4-fluoro-3-phenoxyphenyl)-1,3-dioxolane serves as a key component in the development of pesticides. Its chemical properties allow for the design of effective and targeted pest control solutions.
Used in Organic Chemistry Research:
2-(4-fluoro-3-phenoxyphenyl)-1,3-dioxolane is employed as a reagent or intermediate in various organic synthesis processes. Its versatility in chemical reactions makes it a valuable tool for researchers in the field of organic chemistry.
It is important to handle and store 2-(4-fluoro-3-phenoxyphenyl)-1,3-dioxolane with care due to potential health and safety risks if not managed properly.
Check Digit Verification of cas no
The CAS Registry Mumber 77771-05-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,7 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 77771-05:
(7*7)+(6*7)+(5*7)+(4*7)+(3*1)+(2*0)+(1*5)=162
162 % 10 = 2
So 77771-05-2 is a valid CAS Registry Number.
77771-05-2Relevant academic research and scientific papers
Ligand free, highly efficient synthesis of diaryl ether over copper fluorapatite as heterogeneous reusable catalyst
Mulla, Shafeek A.R.,Inamdar, Suleman M.,Pathan, Mohsinkhan Y.,Chavan, Santosh S.
experimental part, p. 1826 - 1829 (2012/05/04)
A novel ligand-free, highly efficient, and an inexpensive method has been developed by using ecofriendly, heterogeneous reusable copper fluorapatite (CuFAP) catalyst for the synthesis of diaryl ethers from the cross coupling reaction of the various substituted aryl halides (fluoride, chloride, bromide, and iodide) with the potassium salts of various substituted phenols in the presence of N-methyl 2-pyrrolidone (NMP) as a solvent at 120 °C. The protocol obtained the corresponding cross coupling products in good to excellent yield. The CuFAP catalyst was recovered by simple filtration from the reaction mixture and reused several times without the loss of catalytic activity.
