66274-77-9

Basic information

• Product Name: 3'-Cytidylic acid, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-, mono(4-chlorophenyl) ester
• CAS NO: 66274-77-9
• Molecular Formula: C43H39ClN3O10P
• Molecular Weight: 824.224
• Mol File: 66274-77-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3'-Cytidylic acid, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-, mono(4-chlorophenyl) ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-Cytidylic acid, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-, mono(4-chlorophenyl) ester(66274-77-9)
• EPA Substance Registry System: 3'-Cytidylic acid, N-benzoyl-5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-, mono(4-chlorophenyl) ester(66274-77-9)

Safety Data

• Hazardous Substances Data: 66274-77-9(Hazardous Substances Data)

Upstream product

• 13388-88-0 4-chlorophenyl phosphate 
• 67219-55-0 4-N-Benzoyl-2'-deoxy-5'-O-(4,4'-dimethoxytrityl)cytidine 
• 772-79-2 4-chlorophenylphosphorodichloridate 
• 110237-98-4 5'-(4,4'-dimethoxytrityl)-N⁴-benzoyl-2'-deoxycytidine-3'-H-phosphonate 
• 106-48-9 4-chloro-phenol 

Downstream Products

• 83161-01-7 C₆₀H₅₅ClN₅O₁₅P 
• 83160-99-0 C₆₆H₅₈ClN₆O₁₅P 
• 71459-55-7 N-benzoyl-5'-O-(bis(4-methoxyphenyl)phenylmethyl)-P-(4-chlorophenyl)-2'-deoxycytidylyl-(3'->5')-N-benzoyl-2'-deoxy-3'-adenylic acid, 4-chlorophenyl 2-cyanoethyl ester 
• 71459-56-8 C₆₈H₆₁Cl₂N₇O₁₇P₂ 
• 68834-22-0 C₉₀H₈₀Cl₃N₁₀O₂₄P₃ 
• 71459-47-7 dbzC<*>dbzAp(ClPh,CNEt) 
• 71459-48-8 C₄₇H₄₃Cl₂N₇O₁₅P₂ 
• 115584-68-4 Benzoic acid (2R,3S,5R)-2-[[(2R,3S,5R)-5-(4-benzoylamino-2-oxo-2H-pyrimidin-1-yl)-2-hydroxymethyl-tetrahydro-furan-3-yloxy]-(4-chloro-phenoxy)-phosphoryloxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 

Relevant articles and documents

Aryl H-phosphonates. Part 13. A new, general entry to aryl nucleoside phosphate and aryl nucleoside phosphorothioate diesters

The reaction of nucleoside H-phosphonate monoesters with phenols in the presence of a condensing agent, followed by oxidation of the in-situ-generated aryl nucleoside H-phosphonate diesters with iodine-water or with elemental sulfur, provides a new, 'one-

SYNTHESIS OF DEOXYRIBOOLIGONUCLEOTIDES BY USING AROMATIC PHOSPHORAMIDATES AS THE PROTECTING GROUP FOR THE 3'-PHOSPHO ENDS

p-Chlorophenyl phosphoranilidochloridate was used to phosphorylate the 3'-hydroxyl groups of N,5'-O-protected deoxyribonucleotides.These nucleotides served as the 3'-terminal unit in the syntheses of some protected oligonucleotides which were used in a bl