119824-65-6

Basic information

• Product Name: N6-Phenoxyacetyladenosine
• Synonyms: N6-Phenoxyacetyladenosine;N-(Phenoxyacetyl)adenosine
• CAS NO: 119824-65-6
• Molecular Formula: C₁₈H₁₉N₅O₆
• Molecular Weight: 401.37336
• Mol File: 119824-65-6.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: N6-Phenoxyacetyladenosine(CAS DataBase Reference)
• NIST Chemistry Reference: N6-Phenoxyacetyladenosine(119824-65-6)
• EPA Substance Registry System: N6-Phenoxyacetyladenosine(119824-65-6)

Safety Data

• Hazardous Substances Data: 119824-65-6(Hazardous Substances Data)

Upstream product

• 10457-15-5 O^2'_,O3'_,O5'-tris-trimethylsilanyl-adenosine 
• 701-99-5 Phenoxyacetyl chloride 
• 58-61-7 adenosine 
• 110009-60-4 1-(phenoxyacetyl)-1H-imidazole 
• 87792-02-7 9-[3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-1-β-D-arabinofuranosyl]adenine 
• 88121-25-9 9-[3′,5′-O-(1,1,3,3-tetraisopropyldisiloxyl)-2′-O-trifluormethylsulfonyl-β-D-arabinofuranosyl]adenine 
• 203866-59-5 2-[(2R,3R,3aR,9aR)-2-(6-Amino-purin-9-yl)-5,5,7,7-tetraisopropyl-tetrahydro-1,4,6,8-tetraoxa-5,7-disila-cyclopentacycloocten-3-yloxy]-isoindole-1,3-dione 
• 5536-17-4 arabinosyl adenine 
• 14316-61-1 phenoxyacetic anhydride 
• 122-59-8 2-phenoxyacetic acid 

Downstream Products

• 162825-87-8 2',3'-O-methoxymethylidene-N⁶-phenoxyacetyladenosine 
• 121058-83-1 5′-O-(dimethoxytrityl)-2′-O-(tert-butyldimethylsilyl)-N⁶-phenoxyacetyladenosine 
• 121058-86-4 Diisopropyl-phosphoramidous acid (2R,3R,4R,5R)-2-[bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-(tert-butyl-dimethyl-silanyloxy)-5-[6-(2-phenoxy-acetylamino)-purin-9-yl]-tetrahydro-furan-3-yl ester 2-cyano-ethyl ester 
• 1293390-62-1 N₆-(phenoxyacetyl)-2'-O-(tetrahydro-4-methoxy-2H-pyran-4-yl)adenosine 
• 1293390-66-5 N₆-(phenoxyacetyl)-2'-O-(tetrahydro-4-methoxy-2H-pyran-4-yl)adenosine 5'-[2-(2-nitrophenyl)propyl carbonate] 
• 1293390-73-4 N₆-(phenoxyacetyl)-2'-O-(tetrahydro-4-methoxy-2H-pyran-4-yl)adenosine 3'-(2-cyanoethyl N,N-diisopropylphosphoramidite) 5'-[2-(2-nitrophenyl)propyl carbonate] 
• 119824-69-0 Diisopropyl-phosphoramidous acid (2R,3R,4R,5R)-4-(tert-butyl-dimethyl-silanyloxy)-2-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-5-[6-(2-phenoxy-acetylamino)-purin-9-yl]-tetrahydro-furan-3-yl ester methyl ester 
• 119854-42-1 5'-monomethoxytrityl-N-phenoxyacetyl-2'-t-butyldimethylsilyladenosine 
• 201667-42-7 N-(9-{(2R,3R,4R,5R)-5-[Bis-(4-methoxy-phenyl)-phenyl-methoxymethyl]-4-hydroxy-3-methylsulfanylmethoxy-tetrahydro-furan-2-yl}-9H-purin-6-yl)-2-phenoxy-acetamide 
• 201667-28-9 N⁶-phenoxyacetyl-3’,5’-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)-2’-O-(methylthiomethyl)adenosine 
• 201667-32-5 N-[9-((2R,3R,4R,5R)-4-Hydroxy-5-hydroxymethyl-3-methylsulfanylmethoxy-tetrahydro-furan-2-yl)-9H-purin-6-yl]-2-phenoxy-acetamide 
• 131474-68-5 N⁶-phenoxyacetyl-3',5'-O-(1,1,3,3-tetraisopropyldisiloxane-1,3-diyl)adenosine 
• 124328-55-8 N-(9-{(2R,3R,4S,5R)-3,4-Dihydroxy-5-[(4-methoxy-phenyl)-diphenyl-methoxymethyl]-tetrahydro-furan-2-yl}-9H-purin-6-yl)-2-phenoxy-acetamide 
• 121076-16-2 5'-O-dimethoxytrityl-N₆-phenoxyacetyladenosine 

Relevant articles and documents

An improved method for the synthesis of N-phenoxyacetylribonucleosides

N-phenoxyacetylribonucleosides were prepared efficiently from the reaction of ribonucleosides with phenoxyacetylchloride and 1,2,4-triazole (for adenosine and cytidine) or 1-hydroxybenzotriazole (for guanosine).

Nucleotides part LXXIX1: New building blocks for photolithographic syntheses of oligoribonucleotides

Two series of new ribonucleoside 3′-phosphoramidites (see 36-42) carrying the photolabile [2-(2-nitrophenyl)propoxy]carbonyl group at the 5′-O-position were synthesized and characterized as monomeric building blocks for photolithographic syntheses of RNA

A simple method for N-acylation of adenosine and cytidine nucleosides using carboxylic acids activated in-situ with carbonyldiimidazole

Carboxylic acids are activated with 1,1'-carbonyldiimidazole in acetonitrile to form N-acylimidazoles which are then treated with per-trimethylsilyl ethers of nucleosides adenosine or cytidine at ambient temperature to generate exclusively N-acylated-Aden