402859-66-9

Basic information

• Product Name: 1-allyloxy-2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)benzene
• Synonyms: 1-allyloxy-2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)benzene
• CAS NO: 402859-66-9
• Molecular Weight: 458.554
• Mol File: 402859-66-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-allyloxy-2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-allyloxy-2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)benzene(402859-66-9)
• EPA Substance Registry System: 1-allyloxy-2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)benzene(402859-66-9)

Safety Data

• Hazardous Substances Data: 402859-66-9(Hazardous Substances Data)

Upstream product

• 288864-01-7 2-allyloxyphenylmagnesium iodide 
• 223590-99-6 (2S,3S,4S)-3-benzyloxy-4-benzyloxymethyl-2-hydroxymethyl-4-hydroxytetrahydrofuran 
• 10465-78-8 diamide 
• 357436-34-1 1-[2-O-acetyl-3,5-di-O-benzyl-4-(p-toluenesulfonyloxymethyl)-β-D-ribofuranosyl]-2-pyridone 

Downstream Products

• 402859-68-1 2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)1-hydroxybenzene 
• 402859-69-2 1-benzoyloxy-2-(3,5-di-O-benzyl-2-O,4-C-methylene-β-D-ribofuranosyl)benzene 
• 402859-70-5 1-benzoyloxy-2-(2-O,4-C-methylene-β-D-ribofuranosyl)benzene 
• 402859-71-6 1-benzoyloxy-2-[5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl]benzene 
• 1445870-48-3 1-benzoyloxy-2-{3-O-[2-cyanoethoxy(diisopropylamino)phosphino]-5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl}benzene 
• 402859-72-7 2-[5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-b-D-ribofuranosyl]-1-hydroxybenzene 
• 402859-73-8 1-allyloxy-2-[5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl]benzene 
• 402859-74-9 1-allyloxy-2-{3-O-[2-cyanoethoxy(diisopropylamino)phosphino]-5-O-(4,4'-dimethoxytrityl)-2-O,4-C-methylene-β-D-ribofuranosyl}benzene 

Relevant articles and documents

Base-pair recognition ability of hydroxyphenyl nucleobases in parallel triplex DNA

Oligonucleotides containing 2′-deoxyribonucleotides bearing hydroxyphenyl nucleobases or their 2′,4′-BNA-modified analogs were synthesized, and the triplex-forming ability of their oligonucleotides with double-stranded DNA targets was evaluated by UV melt