127682-75-1

Basic information

• Product Name: [(2S,5R)-5-(6-amino-3H-purin-3-yl)tetrahydrofuran-2-yl]methanol
• CAS NO: 127682-75-1
• Molecular Formula: C₁₀H₁₃N₅O₂
• Molecular Weight: 235.2425
• Mol File: 127682-75-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 409°C at 760 mmHg
• Flash Point: 201.2°C
• Density: 1.76g/cm³
• Vapor Pressure: 2.14E-08mmHg at 25°C
• Refractive Index: 1.822
• CAS DataBase Reference: [(2S,5R)-5-(6-amino-3H-purin-3-yl)tetrahydrofuran-2-yl]methanol(CAS DataBase Reference)
• NIST Chemistry Reference: [(2S,5R)-5-(6-amino-3H-purin-3-yl)tetrahydrofuran-2-yl]methanol(127682-75-1)
• EPA Substance Registry System: [(2S,5R)-5-(6-amino-3H-purin-3-yl)tetrahydrofuran-2-yl]methanol(127682-75-1)

Safety Data

• Hazardous Substances Data: 127682-75-1(Hazardous Substances Data)

Upstream product

• 142941-43-3 (3'R,5'R)-9-<5'-<(benzyloxy)methyl>tetrahydrofuran-3'-yl>9H-purin-6-amine 
• 127682-78-4 (2R-trans)-tetrahydro-4-[[(4-methylphenyl)-sulfonyl]oxy]-2-furanmethanol 
• 66224-66-6 adenine 
• 38166-60-8 1,2:5,6-di-O-isopropylidene-α-L-glucofuranoside 
• 127682-82-0 (2R-cis)-4-(6-chloro-9H-purin-9-yl)-tetrahydro-2-furanmethanol 
• 75-09-2 dichloromethane 
• 584-08-7 potassium carbonate 
• 127682-81-9 (2R-cis)-4-[(5-amino-6-chloro-4-pyrimidinyl)-amino]tetrahydro-2-furanmethanol 
• 127682-76-2 (2R,4S)-4-hydroxy-2-dimethoxymethyltetrahydrofuran 
• 127682-80-8 (2R-cis)-4-aminotetrahydro-2-furanmethanol 
• 3396-72-3 3-deoxy-1,2-O-(1-methylethylidene)-α-D-erythro-pentofuranose 4-methylbenzenesufonate 
• 100638-80-0 1,2:5,6-di-O-isopropylidene-3-O-(methylthio)thiocarbonyl-β-D-idose 
• 163956-65-8 methyl 5-O-benzyl-3-deoxy-L-erythro-pentofuranoside 
• 4613-68-7 (3aS,5R,6aS)-2,2-Dimethyl-tetrahydro-furo[2,3-d][1,3]dioxole-5-carbaldehyde 

Relevant articles and documents

SYNTHESYS OF ISO-DDA, MEMBER OF A NOVEL CLASS OF ANTI-HIV AGENTS

Iso-ddA (3) represents a new class of potential anti-AIDS drugs.Synthetic approaches to this compound involving nucleophilic additions to a novel carbohydrate framework are discussed.

Enantiospecific total synthesis of L-2',3'-dideoxyisonucleosides via regioselective opening of optically active C2-symmetric 1,4-pentadiene bis- epoxide

A new method for the synthesis of L-2',3'-dideoxyisonucleosides is described. The readily available, optically active C2-symmetric bis-epoxide (2S,4S)-1,2:4,5-diepoxypentane (5) was prepared by a short route from readily available starting mate

Enantiospecific Synthesis of 3'-Hetero-dideoxy Nucleoside Analogues as Potential Anti-HIV Agents

Two series of analogues of 2',3'-dideoxy carbocyclic nucleosides, in which the 3'-carbon atom is replaced by either an oxygen or a sulfur atom, have been prepared enantiospecifically from diacetone-L-glucose and diacetone-D-glucose respectively.Within eac