121721-05-9

Basic information

• Product Name: 2-(2,4-dinitrophenyl)-4-methyl-1-phenyl-1,2,4a,7a-tetrahydrofuro<3,4-d>pyridazin-5(7H)-one
• Synonyms: 2-(2,4-dinitrophenyl)-4-methyl-1-phenyl-1,2,4a,7a-tetrahydrofuro<3,4-d>pyridazin-5(7H)-one
• CAS NO: 121721-05-9
• Molecular Weight: 396.359
• Mol File: 121721-05-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-(2,4-dinitrophenyl)-4-methyl-1-phenyl-1,2,4a,7a-tetrahydrofuro<3,4-d>pyridazin-5(7H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2,4-dinitrophenyl)-4-methyl-1-phenyl-1,2,4a,7a-tetrahydrofuro<3,4-d>pyridazin-5(7H)-one(121721-05-9)
• EPA Substance Registry System: 2-(2,4-dinitrophenyl)-4-methyl-1-phenyl-1,2,4a,7a-tetrahydrofuro<3,4-d>pyridazin-5(7H)-one(121721-05-9)

Safety Data

• Hazardous Substances Data: 121721-05-9(Hazardous Substances Data)

Upstream product

• 121721-15-1 2-Chloro-3-[(2,4-dinitro-phenyl)-hydrazono]-butyric acid (E)-3-phenyl-allyl ester 
• 74959-17-4 cinnamyl 2-chloroacetoacetate 
• 61363-91-5 (E)-(3-phenylallyl) 3-oxo-butyrate 
• 104-54-1 3-Phenylpropenol 

Relevant articles and documents

Intramolecular Cycloaddition of Azoalkenes Derived from Allylic β-Keto Esters

The 2,4-dinitrophenylhydrazone (2a) of allyl 2-chloroacetoacetate has been prepared and converted into the azoalkene (4a) by reaction with sodium carbonate.The azoalkene undergoes an intramolecular Diels-Alder reaction when heated under reflux in toluene