146609-11-2

Basic information

• Product Name: 1-[(2R,4R)-4-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidine-2,4(1H,3H)-dione
• CAS NO: 146609-11-2
• Molecular Formula: C₉H₁₂N₂O₄
• Molecular Weight: 212.2026
• Mol File: 146609-11-2.mol
• Article Data: 4

Chemical Properties

• Density: 1.397g/cm³
• Refractive Index: 1.566
• CAS DataBase Reference: 1-[(2R,4R)-4-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[(2R,4R)-4-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidine-2,4(1H,3H)-dione(146609-11-2)
• EPA Substance Registry System: 1-[(2R,4R)-4-(hydroxymethyl)tetrahydrofuran-2-yl]pyrimidine-2,4(1H,3H)-dione(146609-11-2)

Safety Data

• Hazardous Substances Data: 146609-11-2(Hazardous Substances Data)

Upstream product

• 133838-13-8 Benzoic acid (3S,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-ylmethyl ester 
• 485815-81-4 Benzoic acid 5-methoxy-tetrahydro-furan-3-ylmethyl ester 
• 133838-13-8 Benzoic acid (3R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-ylmethyl ester 
• 155165-13-2 5(R)-<2,4(1H,3H)-pyrimidinedione>tetrahydro-3(S)-<(((1,1-dimethylethyl)dimethylsilyl)oxy)methyl>furan 
• 155165-11-0 Acetic acid (3S,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-ylmethyl ester 
• 143724-42-9 (rel)-(1S/1R,3S)-(tetrahydro-1-methoxyfuran-3-yl)methanol 
• 99776-32-6 2-(hydroxymethyl)-4,4-dimethoxybutan-1-ol 

Relevant articles and documents

Photochemistry on Soluble Polymer Supports: Synthesis of Nucleosides

(Matrix Presented) A new soluble polymer support synthesis of nucleosides is described. The photochemical ring expansion of cyclobutanones in the presence of poly(ethylene glycol) (PEG) results in polymer-supported ribosides. These photoadducts can be cle

Novel isomeric dideoxynucleosides of the D- and L-apiose family

Short synthetic approaches to optically active, cis and trans dideoxynucleoside analogs of the D- and L-apiose family have been developed. The chiral precursor for the syntheses was the enzymatically prepared compound, S(-)-2-(2-propenyl)-1,3-propanediol monoacetate (5).