153476-69-8 Usage
Uses
Used in Organic Synthesis:
3,5-Dimethyl-2-chloromethylpyridine is used as a key intermediate in the synthesis of various organic compounds. Its unique structure, which includes a pyridine ring and a chloromethyl group, makes it a versatile building block for creating a wide range of chemical products.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, 3,5-dimethyl-2-chloromethylpyridine is utilized as a starting material for the development of new drugs. Its reactivity and structural features allow for the creation of potential therapeutic agents, particularly in the areas of medicinal chemistry and drug design.
Used in Agrochemical Industry:
3,5-Dimethyl-2-chloromethylpyridine also finds application in the agrochemical industry, where it serves as a precursor for the synthesis of pesticides and other crop protection agents. Its chemical properties enable the production of compounds that can effectively manage pests and diseases in agriculture.
Used in Dye and Pigment Industry:
3,5-DIMETHYL-2-CHLOROMETHYLPYRIDINE is employed as a raw material in the production of dyes and pigments, contributing to the coloration of various materials. Its chemical structure allows for the creation of stable and vibrant colors, which are essential in industries such as textiles, plastics, and paints.
Check Digit Verification of cas no
The CAS Registry Mumber 153476-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,7 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 153476-69:
(8*1)+(7*5)+(6*3)+(5*4)+(4*7)+(3*6)+(2*6)+(1*9)=148
148 % 10 = 8
So 153476-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10ClN/c1-6-3-7(2)8(4-9)10-5-6/h3,5H,4H2,1-2H3
153476-69-8Relevant academic research and scientific papers
2--1H-thienoimidazoles. A Novel Class of Gastric H+/K+-ATPase Inhibitors
Weidmann, Klaus,Herling, Andreas W.,Lang, Hans-Jochen,Scheunemann, Karl-Heinz,Rippel, Robert,et al.
, p. 438 - 450 (2007/10/02)
2-thienoimidazoles were synthesized and investigated as potential inhibitors of gastric H+/K+-ATPase.The isomers of the two possible thienoimidazole series were found to be potent inhibitors of gastric acid secretion in vitro and in vivo.Structure-activity relationships indicate that especially lipophilic alkoxy, benzyloxy, and phenoxy substituents with additional electron-demanding properties in the 4-position of the pyridine moiety combined with an unsubstituted thienoimidazole lead to highly active compounds with a favorable chemical stability.Various substitution patterns in the thienoimidazole moiety result in lower biological activity.The heptafluorobutyloxy derivative saviprazole (HOE 731, 5d) was selected for further development and is currently undergoing clinical evaluation.Comprehensive pharmacological studies indicate a pharmacodynamic profile different to omeprazole, the first H+/K+-ATPase blocker introduced on the market.
