6343-58-4 Usage
Uses
Used in Flavoring Agents:
5-methyl-2-(propan-2-yl)pyridine is used as a flavoring agent in the food and beverage industry for its strong, slightly sweet, and nutty aroma, enhancing the taste and aroma profiles of various products.
Used in Pharmaceutical Production:
5-methyl-2-(propan-2-yl)pyridine serves as a key component in the production of pharmaceuticals, where its unique chemical structure contributes to the development of new medications and therapeutic agents.
Used as a Synthetic Intermediate:
5-methyl-2-(propan-2-yl)pyridine is utilized as a synthetic intermediate in organic synthesis, playing a crucial role in the creation of a wide range of chemical products and compounds.
Used in Agrochemical Development:
With potential applications in the development of herbicides and insecticides, 5-methyl-2-(propan-2-yl)pyridine contributes to the advancement of agrochemicals, helping to improve crop protection and management strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 6343-58-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,4 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6343-58:
(6*6)+(5*3)+(4*4)+(3*3)+(2*5)+(1*8)=94
94 % 10 = 4
So 6343-58-4 is a valid CAS Registry Number.
6343-58-4Relevant academic research and scientific papers
Regioselective Addition of Grignard Reagents to 1-Acylpyridinium Salts. A Convenient Method for the Synthesis of 4-Alkyl(aryl)pyridines
Comins, Daniel L.,Abdullah, Abdul H.
, p. 4315 - 4319 (2007/10/02)
The addition of Grignard reagents to 1-acylpyridinium salts afforded 1-acyl-2-alkyl(aryl)-1,2-dihydropyridines and 1-acyl-4-alkyl(aryl)-1,4-dihydropyridines.The regioselectivity of this reaction, 1,2- vs. 1,4-addition, was examined and found to be dependent upon the structures of the Grignard reagent and the 1-acyl group.Pyridine, 2-picoline, and 3-picoline were studied, and in most cases, significant amounts of 1,4-addition occurred.When a catalytic amount of cuprous iodide was present, nearly exclusive 1,4-addition resulted.The crude 1,4-dihydropyridines were aromatized by heating with sulfur to provide 4-substituted pyridines and picolines in good yield and high isomeric purity.
