774556-79-5 Usage
Uses
Used in Scientific Research:
1-(4-BROMOPHENYL)-N-(PYRIDIN-2-YLMETHYL)METHANAMINE is used as a chemical intermediate for the synthesis of other compounds in the field of scientific research. Its unique structure and potential reactivity make it a valuable component in creating new chemical entities.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 1-(4-BROMOPHENYL)-N-(PYRIDIN-2-YLMETHYL)METHANAMINE is used as a potential psychoactive substance for further study. Its structure and properties may lead to the development of new medications targeting neurological or psychiatric conditions.
Used in Chemical Synthesis:
1-(4-BROMOPHENYL)-N-(PYRIDIN-2-YLMETHYL)METHANAMINE is used as a building block in chemical synthesis, particularly for creating novel molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 774556-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,5,5 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 774556-79:
(8*7)+(7*7)+(6*4)+(5*5)+(4*5)+(3*6)+(2*7)+(1*9)=215
215 % 10 = 5
So 774556-79-5 is a valid CAS Registry Number.
774556-79-5Relevant academic research and scientific papers
Singh, Ajeet,Mobin, Shaikh M.,Mathur, Pradeep
, p. 14033 - 14040 (2018)
The synthesis of pyridine alcohol based ruthenium carbonyl clusters Ru3(hep)2(CO)8 (1), Ru3(hpp)2(CO)8 (2), and Ru3(bhmp-H)2(CO)8 (3) {hep-H = 2-(2-hydroxyethyl)pyridine, hpp-H = 2-(3-hydroxypropyl)pyridine and bhmp-H2 = 2,6-bis(hydroxymethyl)pyridine} has been carried out by the reaction of the corresponding pyridine-alcohol ligands with Ru3(CO)12. Clusters 1-3 have been characterized using elemental analysis, NMR, FT-IR, mass spectrometry and single-crystal X-ray structures. The clusters were explored for the selective catalytic transformation of primary amines into secondary amines using alcohols as the mono-alkylating agents via hydrogen transfer reactions. All three display efficient catalytic activity with 1 being the most effective.
