91225-69-3

Usage

Uses

Used in Organic Synthesis:
2-(CHLOROMETHYL)-5-(4-CHLOROPHENYL)THIENO[2,3-D]PYRIMIDIN-4(3H)-ONE is used as a building block in organic synthesis for the creation of various chemical compounds. Its unique structure and functional groups allow for the formation of new molecules with potential applications in different fields.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-(CHLOROMETHYL)-5-(4-CHLOROPHENYL)THIENO[2,3-D]PYRIMIDIN-4(3H)-ONE is used as a key component in the development of new pharmaceuticals. Its structural properties make it a valuable asset in designing drugs that can target specific biological pathways and treat various diseases.
Used in Research and Development:
2-(CHLOROMETHYL)-5-(4-CHLOROPHENYL)THIENO[2,3-D]PYRIMIDIN-4(3H)-ONE is also utilized in research and development activities to study its pharmacological and toxicological properties. This helps in understanding its potential as a therapeutic agent and its safety profile for use in medicine.

InChI:InChI=1/C13H8Cl2N2OS/c14-5-10-16-12(18)11-9(6-19-13(11)17-10)7-1-3-8(15)4-2-7/h1-4,6H,5H2,(H,16,17,18)

Upstream product

• 65234-09-5 ethyl 2-amino-4-chlorophenyl-thiophene-3-carboxylate 
• 107-14-2 chloroacetonitrile 

Downstream Products

• 1419183-50-8 2-fluoromethyl-5-(4-chlorophenyl)thieno[2,3-d]pyrimidin-4(3H)-one 
• 1499192-12-9 5-(4-chlorophenyl)-2-[1-(4-fluorophenyl)-4-oxoazetidin-2-yl]thieno[2,3-d]pyrimidin-4(3H)-one 
• 1499192-11-8 5-(4-chlorophenyl)-2-[1-(4-methylphenyl)-4-oxoazetidin-2-yl]thieno[2,3-d]pyrimidin-4(3H)-one 
• 1499192-10-7 5-(4-chlorophenyl)-2-[1-(2-methylphenyl)-4-oxoazetidin-2-yl]thieno[2,3-d]pyrimidin-4(3H)-one 
• 1499192-09-4 5-(4-chlorophenyl)-2-[1-phenyl-4-oxoazetidin-2-yl]thieno[2,3-d]pyrimidin-4(3H)-one 
• 1499192-02-7 C₂₁H₁₄Cl₂FN₃O₂S 
• 1499192-01-6 C₂₂H₁₇Cl₂N₃O₂S 
• 1499191-99-9 C₂₁H₁₅Cl₂N₃O₂S 
• 900490-94-0 C₁₉H₁₃ClFN₃OS 
• 900490-74-6 C₂₀H₁₆ClN₃OS 
• 900490-76-8 C₂₀H₁₆ClN₃OS 
• 900490-72-4 C₁₉H₁₄ClN₃OS 
• 1415755-81-5 C₂₁H₁₅ClN₄O₂S₂ 
• 1415755-80-4 C₂₀H₁₃ClN₄OS₂ 

Relevant academic research and scientific papers

Synthesis and biological evaluation of novel condensed pyrimidinylmethylsulfinylbenzimidazoles as antiulcer agent

Current therapies to treat gastroesophageal reflux disease (GERD), peptic ulcer disease (PUD), and other acid-related diseases either prevent stimulation of the parietal cell (H2-receptor antagonists) or inhibit gastric H+/K+/s

Design, synthesis, and antihyperlipidemic evaluation of novel 2-[1-(Substitutedphenyl)-4-oxo-azetidin-2-yl]-5,6-disubstitutedthieno[2,3-d] pyrimidin-4(3H)-ones

Novel thienopyrimidine derivatives of azetidinone possessing the combined features of the cholesterol absorption inhibitor drug ezetimibe and potential antihyperlipidemic 2-substitutedthienopyrimidin-4-ones were synthesized and characterized by spectrosco

Synthesis and antihyperlipidemic activity of some novel condensed 2-chloroalkyl-4-chloro/hydroxy-5,6-disubstituted pyrimidines

Synthesis and antihyperlipidemic activity of a series of novel condensed 2-chloroalkyl-4-chloro/hydroxy-5,6-di-substituted pyrimidines are described. The design of these compounds is based on the earlier QSAR study on the antihyperlipidemic 2-substituted

Reaction of Nitriles Under Acidic Conditions. Part III. A Facile Synthesis of Thienopyrimidin-4(3H)-ones

A variety of thiophene o-aminoesters were reacted with cyanates, thiocyanates, cyanamides, acyl cyanides and α-functionalized acetonitrile derivatives to yield the corresponding 2-substituted thienopyrimidin-4(3H)-ones.