26783-32-4

Basic information

• Product Name: Adenosine, 2-amino-N-(phenylmethyl)-
• CAS NO: 26783-32-4
• Molecular Formula: C17H20N6O4
• Molecular Weight: 372.384
• Mol File: 26783-32-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Adenosine, 2-amino-N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Adenosine, 2-amino-N-(phenylmethyl)-(26783-32-4)
• EPA Substance Registry System: Adenosine, 2-amino-N-(phenylmethyl)-(26783-32-4)

Safety Data

• Hazardous Substances Data: 26783-32-4(Hazardous Substances Data)

Upstream product

• 362-76-5 2',3'-isopropylideneguanosine 
• 87619-81-6 2',3'-O-isopropylidene-5'-O-(tert-butyldimethylsilyl)guanosine 
• 705255-05-6 5'-O-(tert-butyldimethylsilyl)-2',3'-O-isopropylidene-2-N-tritylguanosine 
• 705255-06-7 6-(1H-imidazol-1-yl)-2-amino-9-(β-D-ribofuranosyl)purine 
• 100-46-9 benzylamine 
• 2004-07-1 2-Amino-6-chloropurine riboside 

Downstream Products

• 4014-90-8 2-amino-6-benzylaminopurine 

Relevant articles and documents

Functionalization of Guanosine and 2′-Deoxyguanosine at C6: A Modified Appel Process and SNAr Displacement of Imidazole

Treatment of sugar-protected 2-N-trityl derivatives of guanosine and 2′-deoxyguanosine with imidazole/triphenylphosphine/iodine/ethyldiisopropylamine gives the corresponding 6-(imidazol-1-yl)-2-(tritylamino)purine nucleosides. S NAr displacement of the imidazole moiety with nucleophiles provides 2-amino-6-substituted-purine nucleosides and 2′-deoxynucleosides.