7306-79-8 Usage
Uses
Used in Pharmaceutical Industry:
2,4-BIS(BENZYLOXY)PYRIMIDINE is used as a key intermediate for the synthesis of various pharmaceuticals. Its reactivity and structural features make it instrumental in the development of new drugs and medicinal compounds, contributing to the advancement of healthcare and treatment options.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-BIS(BENZYLOXY)PYRIMIDINE is utilized as a building block for the creation of agrochemicals. Its role in this industry is pivotal for the synthesis of pesticides, herbicides, and other agricultural chemicals that are essential for crop protection and yield enhancement.
Used in Fine Chemicals Production:
2,4-BIS(BENZYLOXY)PYRIMIDINE is employed as a critical component in the production of fine chemicals. Its versatility in chemical reactions allows for the creation of specialty chemicals used in various applications, including fragrances, dyes, and other high-value products.
Used in Organic Chemistry Research:
As a reagent in organic chemistry, 2,4-BIS(BENZYLOXY)PYRIMIDINE is involved in cross-coupling reactions, nucleophilic substitutions, and other organic transformations. Its high reactivity and unique structure make it an indispensable tool for researchers exploring new chemical pathways and developing innovative synthetic methods.
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 academic research and scientific papers
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.
