886440-14-8

Basic information

• Product Name: hexahydro-2,5-methano-pentalene-3a-carboxylic acid [6-amino-1-(2-hydroxy-3-phenoxy-propyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-amide
• Synonyms: hexahydro-2,5-methano-pentalene-3a-carboxylic acid [6-amino-1-(2-hydroxy-3-phenoxy-propyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-amide
• CAS NO: 886440-14-8
• Molecular Weight: 440.499
• Mol File: 886440-14-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: hexahydro-2,5-methano-pentalene-3a-carboxylic acid [6-amino-1-(2-hydroxy-3-phenoxy-propyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-amide(CAS DataBase Reference)
• NIST Chemistry Reference: hexahydro-2,5-methano-pentalene-3a-carboxylic acid [6-amino-1-(2-hydroxy-3-phenoxy-propyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-amide(886440-14-8)
• EPA Substance Registry System: hexahydro-2,5-methano-pentalene-3a-carboxylic acid [6-amino-1-(2-hydroxy-3-phenoxy-propyl)-2,4-dioxo-1,2,3,4-tetrahydro-pyrimidin-5-yl]-amide(886440-14-8)

Safety Data

• Hazardous Substances Data: 886440-14-8(Hazardous Substances Data)

Upstream product

• 32968-43-7 5-(phenoxymethyl)-2-amino-2-oxazoline 
• 886439-99-2 5,6-diamino-1-(2-hydroxy-3-phenoxypropyl)uracil 
• 67064-09-9 3-noradamantanecarboxylic acid chloride 
• 886439-97-0 6-amino-5-nitroso-1-(2-hydroxy-3-phenoxypropyl)uracil 
• 886439-95-8 5-amino-6-nitroso-2-phenoxymethyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one 
• 886439-93-6 5-amino-2-phenoxymethyl-2,3-dihydro-oxazolo[3,2-a]pyrimidin-7-one 

Downstream Products

• 886439-62-9 8-(hexahydro-2,5-methano-pentalen-3a-yl)-3-(2-hydroxy-3-phenoxy-propyl)-3,7-dihydro-purine-2,6-dione 
• 886440-23-9 2,2-dimethyl-propionic acid 8-(hexahydro-2,5-methano-pentalen-3a-yl)-3-(2-hydroxy-3-phenoxy-propyl)-2,6-dioxo-1-propyl-1,2,3,6-tetrahydro-purin-7-ylmethyl ester 
• 886440-18-2 2,2-dimethyl-propionic acid 8-(hexahydro-2,5-methano-pentalen-3a-yl)-3-(2-hydroxy-3-phenoxy-propyl)-2,6-dioxo-1,2,3,6-tetrahydro-purin-7-ylmethyl ester 

Relevant articles and documents

Synthesis and preliminary evaluation of new 1- and 3-[1-(2-hydroxy-3- phenoxypropyl)]xanthines from 2-amino-2-oxazolines as potential A1 and A2A adenosine receptor antagonists

The development of potent and selective adenosine receptor ligands as potential drugs is an active area of research. Xanthines are one of the most important classes of adenosine receptor antagonists and have been widely developed in terms of affinity and