79039-89-7 Usage
Uses
Used in Pharmaceutical Industry:
1-(4-Chloro-2,6-diMethylpyridin-3-yl)ethan-1-one is used as a synthetic intermediate for the development of various pharmaceutical products. Its unique structural features allow for the creation of a wide range of compounds with different therapeutic applications, contributing to the advancement of medicine.
Used in Agrochemical Industry:
In the agrochemical sector, 1-(4-Chloro-2,6-diMethylpyridin-3-yl)ethan-1-one serves as a key intermediate in the synthesis of compounds used in agriculture. These compounds may have applications in pest control, crop protection, and other areas related to enhancing agricultural productivity and sustainability.
Potential for Pharmacological Studies:
Due to its potential biological activity, 1-(4-Chloro-2,6-diMethylpyridin-3-yl)ethan-1-one may be studied for its pharmacological properties. This could lead to the discovery of new therapeutic agents or contribute to the understanding of certain biological processes, further expanding the compound's utility in the field of medicine.
Check Digit Verification of cas no
The CAS Registry Mumber 79039-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,3 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79039-89:
(7*7)+(6*9)+(5*0)+(4*3)+(3*9)+(2*8)+(1*9)=167
167 % 10 = 7
So 79039-89-7 is a valid CAS Registry Number.
79039-89-7Relevant academic research and scientific papers
Structure-activity relationships of imidazo[4,5-f]quinoline partial structures and analogs. Discovery of pyrazolo[3,4-f]quinoline derivatives as potent immunostimulants
Moyer,Weber,Gross
, p. 4595 - 4601 (2007/10/02)
Structure-activity studies have been carried out on a series of imidazo[4,5-f]quinoline derivatives reported to have potent in vivo immunostimulatory activity. This activity has been confirmed, and subtle structure-activity relationships have been uncovered which resulted in the identification of novel analogs (pyrazolo[3,4-f]quinoline derivatives, 7a,b) with potent in vivo effects in a mouse protection model. Regioisomeric pyrazolo[4,3-f]quinoline derivatives (6a,b) were shown to be inactive. Data are presented which support the notion that the in vivo activity is mediated by an immunostimulatory mechanism.
Synthesis of Methylpyridine Derivatives. XXXV (1). Reaction of Acetylpyridine with Phosphoryl Chloride to Give Alkynylpyridine
Kato, Tetsuzo,Sato, Masayuki,Wagai, Akihiro
, p. 603 - 606 (2007/10/02)
Reaction of 3-acetyl-4,6-dimethyl-2-(1H)pyridone (9a) with phosphoryl chloride gives 2-chloro-3-ethynyl-4,6-dimethylpyridine (10a). 3-Acetyl-4-hydroxy-6-methyl-2(1H)pyridone (14a) and 3-acetyl-2,6-dimethyl-4-(1H)pyridone (21) undergoes similar reaction to
