39491-47-9

Basic information

• Product Name: (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name)
• Synonyms: β-D-Ribofuranuronamide, 1-(6-amino-9H-purin-9-yl)-1-deoxy-N,N-dimethyl-
• CAS NO: 39491-47-9
• Molecular Formula: C₁₂H₁₆N₆O₄
• Molecular Weight: 308.2932
• Mol File: 39491-47-9.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 687.7°C at 760 mmHg
• Flash Point: 369.7°C
• Density: 1.81g/cm³
• Vapor Pressure: 7.4E-20mmHg at 25°C
• Refractive Index: 1.805
• CAS DataBase Reference: (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name)(39491-47-9)
• EPA Substance Registry System: (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name)(39491-47-9)

Safety Data

• Hazardous Substances Data: 39491-47-9(Hazardous Substances Data)

Usage

Description

(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name) is a complex organic compound featuring a purine ring attached to a tetrahydrofuran ring with two hydroxyl groups and a carboxamide group. The tetrahydrofuran ring is also linked to two N,N-dimethyl groups. (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name) has the potential for various biological activities, including interactions with cellular signaling pathways or enzyme activities. Its specific uses and properties would need to be further studied and determined through experimental research.

Uses

Used in Pharmaceutical Industry:
(2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name) is used as a potential pharmaceutical candidate for [application reason] due to its complex structure and potential for biological activities.
Used in Research and Development:
In the field of research and development, (2S,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxy-N,N-dimethyltetrahydrofuran-2-carboxamide (non-preferred name) is used as a subject of study for understanding its interactions with cellular signaling pathways or enzyme activities, which could lead to the discovery of new therapeutic applications.

Upstream product

• 35788-25-1 2',3;-O-isopropylideneadenosine-5'-(N,N-dimethyl)carboxamide 
• 39491-49-1 2',3'-O-isopropylideneadenosine-5'-carbonyl chloride 

Relevant articles and documents

Modification of the 5' Position of Purine Nucleosides. 2. Synthesis and Some Cardiovascular Properties of Adenosine-5'-(N-substituted)carboxamides

We have shown previously that the esters of adenosine-5'-carboxylic acid (10) represent a new class of potent nontoxic coronary vasodilators.For example, the ethyl ester (12), which is active by an intraduodenal or intravenous route in dogs, causes a larg