1445870-45-0

Basic information

• Product Name: 4-{3-O-[(2-cyanoethoxy)(N,N-diisopropylamino)phosphinyl]-5-O-(4,4'-dimethoxytrityl)-2-deoxy-β-D-erythro-pentofuranosyl}phenyl benzoate
• CAS NO: 1445870-45-0
• Molecular Weight: 816.931
• Mol File: 1445870-45-0.mol

Chemical Properties

• CAS DataBase Reference: 4-{3-O-[(2-cyanoethoxy)(N,N-diisopropylamino)phosphinyl]-5-O-(4,4'-dimethoxytrityl)-2-deoxy-β-D-erythro-pentofuranosyl}phenyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 4-{3-O-[(2-cyanoethoxy)(N,N-diisopropylamino)phosphinyl]-5-O-(4,4'-dimethoxytrityl)-2-deoxy-β-D-erythro-pentofuranosyl}phenyl benzoate(1445870-45-0)
• EPA Substance Registry System: 4-{3-O-[(2-cyanoethoxy)(N,N-diisopropylamino)phosphinyl]-5-O-(4,4'-dimethoxytrityl)-2-deoxy-β-D-erythro-pentofuranosyl}phenyl benzoate(1445870-45-0)

Safety Data

• Hazardous Substances Data: 1445870-45-0(Hazardous Substances Data)

Upstream product

• 1445870-43-8 4-(2-deoxy-β-D-erythro-pentofuranosyl)phenyl benzoate 
• 61807-37-2 benzoic acid 4‐iodophenyl ester 
• 181871-82-9 {(2R,3S)-3-[(tert-butyldimethylsilyl)oxy]-2,3-dihydrofuran-2-yl}methanol 
• 6160-50-5 3,5-di-O-benzyl-2-deoxy-D-ribofuranose 
• 40615-36-9 4,4'-dimethoxytrityl chloride 
• 1445870-41-6 1-benzoyloxy-4-(2-deoxy-3,5-di-O-benzyl-β-D-ribofuranosyl)benzene 
• 1445870-40-5 4-(2-deoxy-3,5-di-O-benzyl-D-ribofuranosyl)-1-hydroxybenzene 
• 1445870-39-2 1-allyloxy-4-(2-deoxy-3,5-di-O-benzyl-D-ribofuranosyl)benzene 

Relevant articles and documents

2,6-Dimercuriphenol as a Bifacial Dinuclear Organometallic Nucleobase

A C-nucleoside having 2,6-dimercuriphenol as the base moiety has been synthesized and incorporated into an oligonucleotide. NMR and UV melting experiments revealed the ability of this bifacial organometallic nucleobase surrogate to form stable dinuclear H

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