73555-93-8

Basic information

• Product Name: N⁶-benzyl-2'-O-(phenylcarbamoyl)adenosine
• Synonyms: N⁶-benzyl-2'-O-(phenylcarbamoyl)adenosine
• CAS NO: 73555-93-8
• Molecular Weight: 476.492
• Mol File: 73555-93-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N⁶-benzyl-2'-O-(phenylcarbamoyl)adenosine(CAS DataBase Reference)
• NIST Chemistry Reference: N⁶-benzyl-2'-O-(phenylcarbamoyl)adenosine(73555-93-8)
• EPA Substance Registry System: N⁶-benzyl-2'-O-(phenylcarbamoyl)adenosine(73555-93-8)

Safety Data

• Hazardous Substances Data: 73555-93-8(Hazardous Substances Data)

Upstream product

• 103-71-9 phenyl isocyanate 
• 4294-16-0 N₆-Benzyladenosine 

Relevant articles and documents

REGIOSELECTIVE (PHENYLCARBAMOYL)ATION OF POLYHYDROXY COMPOUNDS BY PHENYL ISOCYANATE-ZINC NAPHTENATE

In the presence of zinc naphtenate as the catalyst, the reaction of phenyl isocyanate with 1,2-propanediol and 3,4-isopropylidene-D-mannitol gave the primary phenylcarbamates in high yield. 1,2,6-Hexanetriol was selectively phenylcarbamoylated at O-1 and

BIS(TRIBUTYLTIN) OXIDE-PHENYL ISOCYANATE SYSTEM FOR REGIOSELECTIVE (PHENYLCARBAMOYL)ATION OF PURINE AND PYRIMIDINE RIBONUCLEOSIDES

On benzylaminolysis, 5'-O-benzoyl-N6-benzyladenosine 2',3'-carbonate gave a 3:1 mixture of the corresponding 3'- and 2'-benzylcarbamate (67percent total yield); hydrazinolysis and hydroxaminolysis were, however, unsuccessful.An alternative appr