1050436-21-9

Basic information

• Product Name: 2-(2-methoxy-5-{4-methoxy-3-[3-(4-methylphenyl)-4-oxo-1,3-thiazolan-2-yl]benzyl}phenyl)-3-(4-methylphenyl)-1,3-thiazolan-4-one
• Synonyms: 2-(2-methoxy-5-{4-methoxy-3-[3-(4-methylphenyl)-4-oxo-1,3-thiazolan-2-yl]benzyl}phenyl)-3-(4-methylphenyl)-1,3-thiazolan-4-one
• CAS NO: 1050436-21-9
• Molecular Weight: 610.798
• Mol File: 1050436-21-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(2-methoxy-5-{4-methoxy-3-[3-(4-methylphenyl)-4-oxo-1,3-thiazolan-2-yl]benzyl}phenyl)-3-(4-methylphenyl)-1,3-thiazolan-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-methoxy-5-{4-methoxy-3-[3-(4-methylphenyl)-4-oxo-1,3-thiazolan-2-yl]benzyl}phenyl)-3-(4-methylphenyl)-1,3-thiazolan-4-one(1050436-21-9)
• EPA Substance Registry System: 2-(2-methoxy-5-{4-methoxy-3-[3-(4-methylphenyl)-4-oxo-1,3-thiazolan-2-yl]benzyl}phenyl)-3-(4-methylphenyl)-1,3-thiazolan-4-one(1050436-21-9)

Safety Data

• Hazardous Substances Data: 1050436-21-9(Hazardous Substances Data)

Upstream product

• 19782-48-0 5-(3-formyl-4-methoxybenzyl)-2-methoxybenzaldehyde 
• 106-49-0 p-toluidine 
• 68-11-1 mercaptoacetic acid 

Downstream Products

• 1184912-67-1 5-[(Z)-1-(4-fluorophenyl)methylidene]-2-(5-3-[5-[(Z)-1-(4-fluorophenyl)methylidene]-3-(4-methylphenyl)-4-oxo-1-3-thiazolan-2-yl]-4-methoxybenzyl-2-methoxyphenyl)-3-(4-methylphenyl)-1,3-thiazolan-4-one 

Relevant articles and documents

Synthesis and in vitro study of methylene-bis-tetrahydro[1,3]thiazolo[4,5-c]isoxazoles as potential nematicidal agents

A series of methylene-bis-tetrahydro[1,3]thiazolo[4,5-c]isoxazoles 6 were synthesized by the reaction of chalcone derivative of methylene-bis-thiazolidinone 5 with hydroxylamine hydrochloride. The chemical structures of newly synthesized compounds were el

Synthesis and biological evaluation of novel methylene-bis-thiazolidinone derivatives as potential nematicidal agents

(Chemical Equation Presented) In a one pot procedure, a series of novel methylene-bis-thiazolidinone derivatives 5 and 6 was prepared by condensation of 5-(3-formyl-4-methoxybenzyl)-2-methoxybenzaldehyde 3 with mercapto acids and primary aromatic amines 4