77771-05-2 Usage
General Description
2-(4-fluoro-3-phenoxyphenyl)-1,3-dioxolane is a chemical compound that consists of a dioxolane ring structure with a 4-fluoro-3-phenoxyphenyl group attached to it. It is commonly used in the field of pharmaceuticals and agrochemicals, with potential applications in the development of drugs and pesticides. The compound's unique structure and properties make it a valuable building block for the synthesis of various complex molecules. Its chemical and physical properties, such as solubility and reactivity, make it suitable for a wide range of applications in the field of organic chemistry. Additionally, it is important to handle and store this compound with care, as it may pose 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 articles and documents
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.
