937-73-5 Usage
Uses
Used in Coordination Chemistry and Organometallic Synthesis:
2-(p-Tolyl)pyridine is used as a ligand for the formation of coordination compounds and organometallic complexes. Its ability to coordinate with metal ions provides a foundation for the development of new catalysts and materials with unique properties.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(p-Tolyl)pyridine serves as a key building block for the synthesis of various drugs and pharmaceutical compounds. Its structural features allow for the creation of molecules with specific biological activities, contributing to the discovery of new therapeutic agents.
Used in Materials Science:
2-(p-Tolyl)pyridine has potential applications in materials science, particularly in the development of organic electronic devices and optoelectronic materials. Its electronic properties and compatibility with other organic and inorganic components make it a promising candidate for advancing technologies in these fields.
Check Digit Verification of cas no
The CAS Registry Mumber 937-73-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,3 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 937-73:
(5*9)+(4*3)+(3*7)+(2*7)+(1*3)=95
95 % 10 = 5
So 937-73-5 is a valid CAS Registry Number.
937-73-5Relevant academic research and scientific papers
Synthesis of Heterocyclic Compounds via Enamines. Part 8. Acid-catalysed Transformations in 4,4,6-Trimethyl-1,4-Dihydropyrimidine-2(3H)-thione Derivatives and Related Compounds
Singh, Harjit,Singh, Paramjit
, p. 1013 - 1018 (2007/10/02)
1-Substituted 4,4,6-trimethyl-1,4-dihydropyrimidine-2(3H)-thiones (2) on heating in 11M-HCl at 100-110 deg C are converted into the corresponding 2-substituted-amino-4,6,6-trimethyl-6H-1,3-thiazines (4) and/or thioureas.But at 95-100 deg C, Dimroth rearrangement products, e.g. the corresponding 2-substituted-amino-4,4,6-trimethyl-4H-1,3-thiazenes (3) are formed.
