7306-79-8 Usage
General Description
2,4-BIS(BENZYLOXY)PYRIMIDINE is a chemical compound that belongs to the pyrimidine class. It is a white solid substance with a molecular formula of C20H18N2O2 and a molecular weight of 318.37 g/mol. 2,4-BIS(BENZYLOXY)PYRIMIDINE is commonly used as a building block in chemical synthesis and is a key intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. 2,4-BIS(BENZYLOXY)PYRIMIDINE is known for its high reactivity and is often used as a reagent in organic chemistry reactions, such as cross-coupling reactions, nucleophilic substitutions, and more. Its unique chemical structure and properties make it a valuable component in various industrial and research applications.
Check Digit Verification of cas no
The CAS Registry Mumber 7306-79-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,0 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7306-79:
(6*7)+(5*3)+(4*0)+(3*6)+(2*7)+(1*9)=98
98 % 10 = 8
So 7306-79-8 is a valid CAS Registry Number.
InChI:InChI=1/C18H16N2O2/c1-3-7-15(8-4-1)13-21-17-11-12-19-18(20-17)22-14-16-9-5-2-6-10-16/h1-12H,13-14H2
7306-79-8Relevant articles and documents
Photoreductive Removal of O-Benzyl Groups from Oxyarene N-Heterocycles Assisted by O-Pyridine-pyridone Tautomerism
Todorov, Aleksandar R.,Wirtanen, Tom,Helaja, Juho
, p. 13756 - 13767 (2017/12/26)
Facile photoreductive protocols have been developed to remove benzyl O-protective groups from oxyarene N-heterocycles at positions capable for 2-/4-O-pyridine-2-/4-pyridone tautomerism. Blue light irradiation, a [Ru] or [Ir] photocatalyst, and ascorbic acid in a water-acetonitrile solution debenzylates a variety of aryl N-heterocycles cleanly and selectively. Ascorbic acid has two functions in the reaction. On the one hand, it protonates the N-heterocycles that reduces their reduction potentials notably and on the other hand it acts as a sacrificial reductant. Reduction potentials and free energy barriers calculated at the CPCM-B3LYP/6-31+G? level can predict the reactivities of the studied substrates.
