1033301-29-9

Basic information

• Product Name: 1,3-dimethyl-2,4,6-trioxoperhydropyrimidine-5-spiro-6'-{4'-methoxy-7'-(1,3-dimethyl-5-[2-(4-pyridyl)ethyl]-2,4,6-trioxoperhydropyrimidin-5-yl)-5',6',7',8'-tetrahydro[1,3]dioxolo[4,5-g]naphthalene}
• Synonyms: 1,3-dimethyl-2,4,6-trioxoperhydropyrimidine-5-spiro-6'-{4'-methoxy-7'-(1,3-dimethyl-5-[2-(4-pyridyl)ethyl]-2,4,6-trioxoperhydropyrimidin-5-yl)-5',6',7',8'-tetrahydro[1,3]dioxolo[4,5-g]naphthalene}
• CAS NO: 1033301-29-9
• Molecular Weight: 605.604
• Mol File: 1033301-29-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,3-dimethyl-2,4,6-trioxoperhydropyrimidine-5-spiro-6'-{4'-methoxy-7'-(1,3-dimethyl-5-[2-(4-pyridyl)ethyl]-2,4,6-trioxoperhydropyrimidin-5-yl)-5',6',7',8'-tetrahydro[1,3]dioxolo[4,5-g]naphthalene}(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-dimethyl-2,4,6-trioxoperhydropyrimidine-5-spiro-6'-{4'-methoxy-7'-(1,3-dimethyl-5-[2-(4-pyridyl)ethyl]-2,4,6-trioxoperhydropyrimidin-5-yl)-5',6',7',8'-tetrahydro[1,3]dioxolo[4,5-g]naphthalene}(1033301-29-9)
• EPA Substance Registry System: 1,3-dimethyl-2,4,6-trioxoperhydropyrimidine-5-spiro-6'-{4'-methoxy-7'-(1,3-dimethyl-5-[2-(4-pyridyl)ethyl]-2,4,6-trioxoperhydropyrimidin-5-yl)-5',6',7',8'-tetrahydro[1,3]dioxolo[4,5-g]naphthalene}(1033301-29-9)

Safety Data

• Hazardous Substances Data: 1033301-29-9(Hazardous Substances Data)

Upstream product

• 100-43-6 4-vinylpyridine 
• 471248-47-2 4'-methoxy-1,3-dimethyl-7'-(1,3-dimethyl-2,4,6-trioxoperhydropyrimidin-5-yl)-2,4,6-trioxospiro[perhydropyrimidine-5,6'-(5',6',7',8'-tetrahydro[1,3]dioxolo[4,5-g]naphthalene)] 

Relevant articles and documents

Chemical modification of plant alkaloids. 5. Spirocyclic systems based on cotarnine and barbituric acids

Cotarnine was reacted with barbituric acid and its N-alkylbartituric and 1,3-dimethyl-2-thio analogs under forcing conditions to produce spirocyclic systems. Adducts, further transformations of which included skeletal rearrangements (a type of T-reaction) and subsequent deamination, were formed in the first step. The reaction of N-methylcotarnine and 1,3-dimethylbarbituric acid was analogous. The properties of the spirocyclic products were studied. They were further modified at the CH-acid and aromatic moieties.