120524-47-2

Basic information

• Product Name: (2R,3S,4R,5R)-2-Hydroxymethyl-5-{6-[(naphthalen-1-ylmethyl)-amino]-2-phenylamino-purin-9-yl}-tetrahydro-furan-3,4-diol
• CAS NO: 120524-47-2
• Molecular Weight: 498.541
• Mol File: 120524-47-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3S,4R,5R)-2-Hydroxymethyl-5-{6-[(naphthalen-1-ylmethyl)-amino]-2-phenylamino-purin-9-yl}-tetrahydro-furan-3,4-diol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S,4R,5R)-2-Hydroxymethyl-5-{6-[(naphthalen-1-ylmethyl)-amino]-2-phenylamino-purin-9-yl}-tetrahydro-furan-3,4-diol(120524-47-2)
• EPA Substance Registry System: (2R,3S,4R,5R)-2-Hydroxymethyl-5-{6-[(naphthalen-1-ylmethyl)-amino]-2-phenylamino-purin-9-yl}-tetrahydro-furan-3,4-diol(120524-47-2)

Safety Data

• Hazardous Substances Data: 120524-47-2(Hazardous Substances Data)

Upstream product

• 118-31-0 (naphth-1-yl)methylamine 
• 117325-41-4 (2R,3R,4S,5R)-2-(6-Chloro-2-phenylamino-purin-9-yl)-5-hydroxymethyl-tetrahydro-furan-3,4-diol 

Relevant articles and documents

C2,N6-disubstituted adenosines: synthesis and structure-activity relationships.

Extracellular adenosine receptors have been divided into two major subtypes, called A1 and A2. Substitution of the adenosine molecule with appropriate groups at C2 or N6 is known to impart selectivity for the A2 receptor over the A1 receptor. In the prese