98157-45-0

Basic information

• Product Name: 4H-1,3-Dioxin-4-one, 6-(4-chlorophenyl)-2,2-dimethyl-
• CAS NO: 98157-45-0
• Molecular Formula: C12H11ClO3
• Molecular Weight: 238.671
• Mol File: 98157-45-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4H-1,3-Dioxin-4-one, 6-(4-chlorophenyl)-2,2-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 4H-1,3-Dioxin-4-one, 6-(4-chlorophenyl)-2,2-dimethyl-(98157-45-0)
• EPA Substance Registry System: 4H-1,3-Dioxin-4-one, 6-(4-chlorophenyl)-2,2-dimethyl-(98157-45-0)

Safety Data

• Hazardous Substances Data: 98157-45-0(Hazardous Substances Data)

Upstream product

• 58303-62-1 5-(4-chlorophenyl)-2,3-dihydrofuran-2,3-dione 
• 67-64-1 acetone 

Downstream Products

• 1332639-14-1 (1E,3Z)-4-hydroxy-4-(4-chlorophenyl)-1-(1,3,3-trimethyl-2,3-dihydro-1H-indol-2-ylidene)but-3-en-2-one 
• 63524-45-8 6-(4-chloro-phenyl)-[1,3]oxazine-2,4-dione 
• 140836-13-1 N-(4-Amino-furazan-3-yl)-3-(4-chloro-phenyl)-3-oxo-propionamide 
• 124695-33-6 3-Acetyl-6-(4-chloro-phenyl)-2-methyl-pyran-4-one 
• 105115-37-5 [3-(4-Chloro-phenyl)-3-oxo-propionyl]-carbamic acid ethyl ester 
• 129781-15-3 1-(4-Chloro-phenyl)-2-[3-phenyl-4H-[1,2,4]oxadiazol-(5E)-ylidene]-ethanone 
• 82040-00-4 4-(p-chlorophenyl)-2,3-dihydro-1H-1,5-benzodiazepin-2-one 
• 962-05-0 3-(4-chlorophenyl)-3-oxo-N-phenylpropanamide 
• 127846-42-8 2-[3-(4-Chloro-phenyl)-3-oxo-propionylamino]-benzamide 
• 127846-35-9 C₁₀H₈ClNO₃ 
• 126965-13-7 2-N-phenylguanidino-6-(4-chlorophenyl)-1,3-oxazin-4-one 
• 140836-09-5 3-(4-Chloro-phenyl)-N-{2-[3-(4-chloro-phenyl)-3-oxo-propionylamino]-1,2-bis-[(E)-hydroxyimino]-ethyl}-3-oxo-propionamide 
• 93795-51-8 6-(4-Chloro-phenyl)-2-dibutylamino-[1,3]oxazin-4-one 
• 127846-38-2 N-[3-(4-Chloro-phenyl)-3-oxo-propionyl]-acetamide 

Relevant articles and documents

REACTION OF 2,2-DIMETHYL-6-ARYL-1,3-DIOXIN-4-ONES WITH AROMATIC AMINES AND o-PHENYLENEDIAMINE

N-Arylaroylacetamides and 4-aryl-1,5-benzodiazepin-4-ones were obtained by the thermolysis of 2,2-dimethyl-6-aryl-1,3-dioxin-4-ones in the presence of aromatic amines and o-phenylenediamine respectively.Investigetion of the reaction kinetics showed that the controlling stage is the generation of the aroylketenes, which takes place by a concerted -retrocycloaddition mechanism.