88015-19-4

Basic information

• Product Name: 3'-Guanylic acid, N-benzoyl-2'-O-[(4-methoxyphenyl)methyl]-, 4-chlorophenyl 5-chloro-8-quinolinyl ester
• CAS NO: 88015-19-4
• Molecular Formula: C40H33Cl2N6O10P
• Molecular Weight: 859.616
• Mol File: 88015-19-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 3'-Guanylic acid, N-benzoyl-2'-O-[(4-methoxyphenyl)methyl]-, 4-chlorophenyl 5-chloro-8-quinolinyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3'-Guanylic acid, N-benzoyl-2'-O-[(4-methoxyphenyl)methyl]-, 4-chlorophenyl 5-chloro-8-quinolinyl ester(88015-19-4)
• EPA Substance Registry System: 3'-Guanylic acid, N-benzoyl-2'-O-[(4-methoxyphenyl)methyl]-, 4-chlorophenyl 5-chloro-8-quinolinyl ester(88015-19-4)

Safety Data

• Hazardous Substances Data: 88015-19-4(Hazardous Substances Data)

Upstream product

• 772-79-2 4-chlorophenylphosphorodichloridate 
• 3676-72-0 N²-benzoylguanosine 
• 130-16-5 5-Chloro-8-hydroxyquinoline 
• 77181-80-7 Phosphorochloridic acid 4-chloro-phenyl ester 5-chloro-quinolin-8-yl ester 
• 87985-93-1 N-{9-[(2R,3R,4R,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-3-(4-methoxy-benzyloxy)-tetrahydro-furan-2-yl]-6-oxo-6,9-dihydro-1H-purin-2-yl}-benzamide 
• 80015-56-1 2'-O-(4-methoxybenzyl)-N²-benzoylguanosine 
• 2746-25-0 p-Methoxybenzyl bromide 
• 87985-94-2 Phosphoric acid (2R,3R,4R,5R)-5-(2-benzoylamino-6-oxo-1,6-dihydro-purin-9-yl)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(4-methoxy-benzyloxy)-tetrahydro-furan-3-yl ester 4-chloro-phenyl ester 5-chloro-quinolin-8-yl ester 

Downstream Products

• 87999-43-7 C₈₇H₇₄Cl₃N₉O₂₁P₂ 

Relevant articles and documents

Synthesis of Ribooligonucleotides Using the 4-Methoxybenzyl Group as a New Protecting Group for the 2'-Hydroxyl Group

The 4-methoxybenzyl group was introduced to protect the 2'-hydroxyl group of uridine, cytidine, and N2-benzoylguanosine by treatment of 2',3'-O-(dibutylstannylene)uridine or NaH-treated nucleosides with 4-methoxybenzyl bromide.The 2'-O-(4-methoxybenzyl)nucleosides can be used as useful starting materials for the synthesis of 3',5'-linked ribooligonucleotides.The 4-methoxybenzyl group was removed rapidly from the ribooligonucleotides by treatment with triphenylmethyl fluoroborate, and the completely deblocked ribooligonucleotides were characterized by enzymatic hydrolysis.