6425-65-6 Usage
General Description
Benzene-1,2-diylbis(morpholin-4-ylmethanone) is a chemical compound that belongs to the class of bis-morpholino diarylmethanones. It is a white to off-white powder that is often used in organic synthesis and pharmaceutical research. benzene-1,2-diylbis(morpholin-4-ylmethanone) has various applications, including as a building block in the synthesis of pharmaceuticals and as an intermediate in the preparation of heterocyclic compounds. Its unique structure and properties make it a valuable reagent in the development of new drugs and biologically active compounds. Additionally, it has potential applications in materials science and chemical engineering due to its versatility and reactivity.
Check Digit Verification of cas no
The CAS Registry Mumber 6425-65-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,2 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6425-65:
(6*6)+(5*4)+(4*2)+(3*5)+(2*6)+(1*5)=96
96 % 10 = 6
So 6425-65-6 is a valid CAS Registry Number.
6425-65-6Relevant articles and documents
The aminocarbonylation of 1,2-diiodoarenes with primary and secondary amines catalyzed by palladium complexes with imidazole ligands
Wójcik, Przemys?aw,Trzeciak, Anna M.
, p. 73 - 83 (2018/05/22)
The efficient carbonylative cyclization of 1,2-diiodobenzene with different primary and secondary amines was performed using a palladium complex with an imidazole ligand, PdCl2(BIM)2, as a catalyst. In reactions performed at 1 atm of CO with primary amines, phthalimides were obtained as the only products with yields of up to 100% in 4 h. An even shorter time, 1 h, was sufficient to obtain the same products employing methyl-2-iodobenzoate as a substrate instead of 1,2-diiodobenzene. In an analogous reaction with secondary amines, 1,2-diiodobenzene was converted to three products, formed in amounts dependent on the reaction conditions. The presence of Pd NPs and soluble palladium intermediates indicated their participation in the catalytic reaction.
