10447-76-4 Usage
Uses
Used in Pharmaceutical Industry:
2-(Chloromethyl)-5-ethylpyridine is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the creation of new drug molecules, contributing to the development of novel treatments and therapies.
Used in Agrochemical Industry:
In the agrochemical sector, 2-(Chloromethyl)-5-ethylpyridine serves as an essential intermediate for the production of agrochemicals. Its role in the synthesis process helps in the development of effective pesticides and other agricultural chemicals that protect crops and enhance agricultural productivity.
Used in Dye and Pigment Manufacturing:
2-(Chloromethyl)-5-ethylpyridine is utilized as a building block in the manufacturing of dyes and pigments. Its chemical properties enable the production of a wide range of colors and shades, catering to the diverse needs of various industries such as textiles, plastics, and printing.
Used in Organic Compound Synthesis:
2-(CHLOROMETHYL)-5-ETHYLPYRIDINE is also employed in the synthesis of other organic compounds, broadening its applications across different fields. Its versatility in chemical reactions makes it a valuable component in the production of various specialty chemicals and materials.
Check Digit Verification of cas no
The CAS Registry Mumber 10447-76-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10447-76:
(7*1)+(6*0)+(5*4)+(4*4)+(3*7)+(2*7)+(1*6)=84
84 % 10 = 4
So 10447-76-4 is a valid CAS Registry Number.
10447-76-4Relevant academic research and scientific papers
Thibon, Aurore,Bartoli, Jean-Franois,Bourcier, Sophie,Banse, Frederic
, p. 9587 - 9594 (2009)
The new ligand L624E (N,N,N′,N′- tetrakis(5-ethyl-2-pyridylmethyl)ethane-1,2-diamine) was designed as a more robust analog of TPEN (N,N,N′,N′-tetrakis(2-pyridylmethyl)ethane-1, 2-diamine) for which the ability at stabilizing high valent Fe-Oxo and Fe-(hydro)peroxo has been reported. With respect to the latter, the pyridyl β-substituents in L624E do not modify the Fe coordination chemistry. From the FeII precursor, [FeO]2+ and FeIII-(hydro)peroxo intermediates are prepared using the same synthetic methods as those reported for the TPEN analogs. The spectroscopic characteristics of all L624E-Fe complexes are very similar to their TPEN analog. However, [(L624E)FeO]2+ has a greater lifetime than that of [(TPEN)FeO]2+. This can be explained by a restricted bimolecular autodegradation due to the bulkiness provided by the ethyl substituents. Regarding small organic molecule oxidation, [(L624E)FeO]2+ and [(L6 24E)FeOOH]2+ exhibit behaviours that seem to be general for the complexes built with ligands of the TPEN family: [FeO]2+ appears to be efficient to epoxidize olefins, whereas [FeOOH]2+ hydroxylates the aromatic ring of anisole with efficacy. The Royal Society of Chemistry 2009.
