64723-02-0

Basic information

• Product Name: Adenosine, N-benzoyl-2'-deoxy-, 3',5'-dibenzoate
• CAS NO: 64723-02-0
• Molecular Formula: C31H25N5O6
• Molecular Weight: 563.569
• Mol File: 64723-02-0.mol

Chemical Properties

• CAS DataBase Reference: Adenosine, N-benzoyl-2'-deoxy-, 3',5'-dibenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: Adenosine, N-benzoyl-2'-deoxy-, 3',5'-dibenzoate(64723-02-0)
• EPA Substance Registry System: Adenosine, N-benzoyl-2'-deoxy-, 3',5'-dibenzoate(64723-02-0)

Safety Data

• Hazardous Substances Data: 64723-02-0(Hazardous Substances Data)

Upstream product

• 65-85-0 benzoic acid 
• 958-09-8 2'-deoxy-D-adenosine 
• 98-88-4 benzoyl chloride 

Downstream Products

• 958-09-8 2'-deoxy-D-adenosine 
• 85240-06-8 C₄₉H₄₃Cl₂N₁₁O₁₃P₂ 
• 85240-01-3 C₆₁H₅₅ClN₇O₁₄P 
• 85240-03-5 C₄₂H₄₀Cl₂N₈O₁₄P₂ 
• 73118-61-3 Benzoic acid (2R,3S,5R)-2-[[(2R,3S,5R)-5-(6-benzoylamino-purin-9-yl)-2-hydroxymethyl-tetrahydro-furan-3-yloxy]-(2-chloro-phenoxy)-phosphoryloxymethyl]-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 
• 64325-78-6 N₆-benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine 
• 85240-02-4 C₆₀H₅₅Cl₂N₇O₁₆P₂ 
• 76958-61-7 [1,2,4]Triazol-1-yl-phosphonic acid (2R,3S,5R)-5-(6-benzoylamino-purin-9-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 2-chloro-phenyl ester 
• 78098-91-6 C₆₃H₅₈Cl₂N₈O₁₆P₂ 
• 80817-34-1 N-6-benzoyl-5'-O-(dimethoxytrityl)-2'-deoxyadenosine 3'-(o-chlorophenyl β-cyanoethyl phosphate) 
• 69434-23-7 bzA_dΦ(CNEt) 
• 75269-16-8 <(MeO)2Tr>bzA_dΦbzA_dΦ(CNEt) 
• 78272-53-4 Phosphoric acid (2R,3S,5R)-5-(6-benzoylamino-purin-9-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-tetrahydro-furan-3-yl ester 2-chloro-phenyl ester 
• 4546-72-9 N₆-benzoyl-2'-deoxyadenosine 

Relevant articles and documents

Simplified Liquid-Phase Preparation of Four Decadeoxyribonucleotides and their Preliminary Spectroscopic Characterization

Four self-complementary decadeoxyribonucleotides, dApTpApTpApTpApTpApT,dApTpApTpCpGpApTpApT, dApTpApTpGpCpApTpApT and dApApApApApTpTpTpTpT, were chemically synthesized by the phosphotriester procedure.Efforts were concentrated on keeping the procedure as simple as possible, concomitant with obtaining high-purity products at each step of the process.The decamers were elaborated from the 3'-end, starting with a 3'-O-benzoylated monomer according to the scheme: monomer + monomer -> dimer + dimer -> tetramer + dimer -> hexamer + tetramer -> decamer.Putity of intermediates and of the fully blocked decamers were monitored by chromatography and by 300-MHz 1H-NMR. spectroscopy.The deblocked decadeoxyribonucleotides were characterized by their UV., CD., and 1H-NMR. spectra.