155831-90-6

Basic information

• Product Name: 2'-O-T-BUTYLDIMETHYLSILYL-3'-O-[(DIISOPROPYLAMINO)(2-CYANOETHOXY)PHOSPHINO]-5'-O-(4,4'-DIMETHOXYTRITYL)-2(1H)-PYRIMIDINONE-1-BETA-D-RIBOSIDE
• Synonyms: 2'-O-T-BUTYLDIMETHYLSILYL-3'-O-[(DIISOPROPYLAMINO)(2-CYANOETHOXY)PHOSPHINO]-5'-O-(4,4'-DIMETHOXYTRITYL)-2(1H)-PYRIMIDINONE-1-BETA-D-RIBOSIDE;4HC CEP;ZEBULARINE CEP;1-[5-O-[Bis(4-methoxyphenyl)phenylmethyl]-3-O-[[bis(1-methylethyl)amino](2-cyanoethoxy)phosphino]-2-O-[(1,1-dimethylethyl)dimethylsilyl]-beta-D-ribofuranosyl]-2(1H)-pyrimidinone;Zebularine 3'-CE phosphoramidite
• CAS NO: 155831-90-6
• Molecular Formula: C45H61N4O8PSi
• Molecular Weight: 845.05
• Mol File: 155831-90-6.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2'-O-T-BUTYLDIMETHYLSILYL-3'-O-[(DIISOPROPYLAMINO)(2-CYANOETHOXY)PHOSPHINO]-5'-O-(4,4'-DIMETHOXYTRITYL)-2(1H)-PYRIMIDINONE-1-BETA-D-RIBOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2'-O-T-BUTYLDIMETHYLSILYL-3'-O-[(DIISOPROPYLAMINO)(2-CYANOETHOXY)PHOSPHINO]-5'-O-(4,4'-DIMETHOXYTRITYL)-2(1H)-PYRIMIDINONE-1-BETA-D-RIBOSIDE(155831-90-6)
• EPA Substance Registry System: 2'-O-T-BUTYLDIMETHYLSILYL-3'-O-[(DIISOPROPYLAMINO)(2-CYANOETHOXY)PHOSPHINO]-5'-O-(4,4'-DIMETHOXYTRITYL)-2(1H)-PYRIMIDINONE-1-BETA-D-RIBOSIDE(155831-90-6)

Safety Data

• Hazardous Substances Data: 155831-90-6(Hazardous Substances Data)

Usage

Uses

Zebularine CEP (CAS# 155831-90-6) is a fluorescent nucleotide, and has been incorporated into oligoribonucleotides to form a useful probe for the exocyclic amino function in cytidine.

Upstream product

• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 
• 52523-24-7 (2R,3R,4R,5R)-2-((benzoyloxy)methyl)-5-(2-oxopyrimidin-1(2H)-yl)tetrahydrofuran-3,4-diyl dibenzoate 
• 3690-10-6 Zebularine 
• 170660-47-6 2-pyrimidinone-1-β-D-(5'-O-dimethoxytritylriboside) 
• 124482-92-4 2-cyanoethyl-N,N-(diisopropylamino)chlorophosphine 
• 170660-44-3 2-pyrimidinone-1-β-D-(2'-O-t-butyldimethylsilyl-5'-O-dimethoxytritylriboside) 
• 102691-36-1 N,N,N',N'-tetraisopropyl 2-cyanoethylphosphorodiamidite 

Relevant articles and documents

Atomic group 'mutagenesis' reveals major groove fine interactions of a tRNA synthetase with an RNA helix

RNA discrimination by aminoacyl-tRNA synthetases involves both major and minor groove interactions with the acceptor stem domain of tRNA substrates. In the case of class II Escherichia coli alanyl-tRNA synthetase (AlaRS), minor groove atomic groups in and