168424-15-5

Basic information

• Product Name: 5-(2',3',5'-Tri-O-benzyl-β-D-ribofuranosyl)-3,6-bis(trifluormethyl)-1,2,4-triazin
• CAS NO: 168424-15-5
• Molecular Weight: 619.563
• Mol File: 168424-15-5.mol

Chemical Properties

• CAS DataBase Reference: 5-(2',3',5'-Tri-O-benzyl-β-D-ribofuranosyl)-3,6-bis(trifluormethyl)-1,2,4-triazin(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(2',3',5'-Tri-O-benzyl-β-D-ribofuranosyl)-3,6-bis(trifluormethyl)-1,2,4-triazin(168424-15-5)
• EPA Substance Registry System: 5-(2',3',5'-Tri-O-benzyl-β-D-ribofuranosyl)-3,6-bis(trifluormethyl)-1,2,4-triazin(168424-15-5)

Safety Data

• Hazardous Substances Data: 168424-15-5(Hazardous Substances Data)

Upstream product

• 16453-18-2 3,6-bis(trifluoromethyl)-1,2,4,5-tetrazine 
• 168424-13-3 2,5-Anhydro-3,4,6-tri-O-benzyl-imidoallonsaeuremethylester 
• 75172-84-8 2,3,5-tri-O-benzyl-1-O-(p-nitrobenzoyl)-α,β-D-ribofuranose 
• 82267-01-4 (2S,3S,4R,5R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-carbonitrile 

Relevant articles and documents

Synthesis of the first 1,2,4-triazine C-nucleoside and its transformation to novel pyridine C-nucleosides by 'inverse' [4 + 2]-cycloaddition reactions

The anomeric C-glycosyl precursors 6 and 7, appropriate for C-nucleoside synthesis and functionalized by an imidate group, were prepared. They were utilized as heterodienophiles in a Diels-Alder reaction with inverse electron demand to yield the O-benzyl