130195-61-8

Basic information

• Product Name: 3,4,5,7-Tetrahydro-1,3-dimethyl-2,6-dioxo-anti-10,syn-11-diphenyl-4,5-ethano-1H-purin-7-carbonsaeure-ethylester
• Synonyms: 3,4,5,7-Tetrahydro-1,3-dimethyl-2,6-dioxo-anti-10,syn-11-diphenyl-4,5-ethano-1H-purin-7-carbonsaeure-ethylester
• CAS NO: 130195-61-8
• Molecular Weight: 432.479
• Mol File: 130195-61-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3,4,5,7-Tetrahydro-1,3-dimethyl-2,6-dioxo-anti-10,syn-11-diphenyl-4,5-ethano-1H-purin-7-carbonsaeure-ethylester(CAS DataBase Reference)
• NIST Chemistry Reference: 3,4,5,7-Tetrahydro-1,3-dimethyl-2,6-dioxo-anti-10,syn-11-diphenyl-4,5-ethano-1H-purin-7-carbonsaeure-ethylester(130195-61-8)
• EPA Substance Registry System: 3,4,5,7-Tetrahydro-1,3-dimethyl-2,6-dioxo-anti-10,syn-11-diphenyl-4,5-ethano-1H-purin-7-carbonsaeure-ethylester(130195-61-8)

Safety Data

• Hazardous Substances Data: 130195-61-8(Hazardous Substances Data)

Upstream product

• 101774-91-8 3,7-Dihydro-1,3-dimethyl-2,6-dioxo-1H-purin-7-carbonsaeure-ethylester 
• 103-30-0 (E)-1,2-diphenyl-ethene 

Relevant articles and documents

Selectivities in Photoadditions with Multifunctional Caffeine Derivatives

Electronically excited stilbene (21*), 4,4'-dichlorostilbene (1*), and 4,4'-dimethoxystilbene (18*) are trapped by caffeine derivatives 2, 13, or 22 with variable results.While 1* and 2 react predominantly at the imino double bond (substitutive and fragmentating additions), 1* or 18* and 13 produce mostly propellanes by photocycloaddition, which hydrolyze or may be hydrolyzed. 21* and the relatively electron-poor compound 22 produce mostly propellanes, which always show a preponderance of the syn-10,anti-11 stereoisomers.These selectivities as well as the competition with reactions at the imino double bonds are rationalized on the basis of diradical mechanisms with the aid of semiempirical AM1 calculations.Earlier results on closely related transformations are also discussed.