5856-57-5

Basic information

• Product Name: 1-(5-O-carbamoyl-2-deoxypentofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione
• CAS NO: 5856-57-5
• Molecular Formula: C₁₁H₁₅N₃O₆
• Molecular Weight: 285.2533
• Mol File: 5856-57-5.mol
• Article Data: 1

Chemical Properties

• Density: 1.478g/cm³
• Refractive Index: 1.58
• CAS DataBase Reference: 1-(5-O-carbamoyl-2-deoxypentofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5-O-carbamoyl-2-deoxypentofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione(5856-57-5)
• EPA Substance Registry System: 1-(5-O-carbamoyl-2-deoxypentofuranosyl)-5-methylpyrimidine-2,4(1H,3H)-dione(5856-57-5)

Safety Data

• Hazardous Substances Data: 5856-57-5(Hazardous Substances Data)

Usage

Chemical structure

A nucleoside analog consisting of a sugar molecule attached to a nitrogenous base.

Unique features

Carbamoyl group at the 5' position of the sugar molecule and a methyl group on the pyrimidine ring.

Applications

Potential use in antiviral and anticancer therapies.

Mechanism of action

Interference with nucleic acid synthesis and inhibition of growth in rapidly dividing cells.

Importance

Understanding the structure and properties can provide insights into its biological and pharmaceutical activities.

Upstream product

• 50-89-5 thymidine 
• 146457-45-6 Carbonic acid (2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-ylmethyl ester vinyl ester 

Relevant articles and documents

Chemo-enzymatic synthesis of 2′-deoxynucleoside urethanes

2′-Deoxynucleoside 5′- and 3′-(N-alkyl) carbamates were synthesized in a two step procedure, asing lipases to catalyze the first regioselective vinyloxycarbonylation step.