22432-96-8

Basic information

• Product Name: 1-pentofuranosyl-1,3,5-triazinane-2,4,6-trione
• CAS NO: 22432-96-8
• Molecular Formula: C₈H₁₁N₃O₇
• Molecular Weight: 261.1888
• Mol File: 22432-96-8.mol
• Article Data: 2

Chemical Properties

• Density: 1.8g/cm³
• Refractive Index: 1.636
• CAS DataBase Reference: 1-pentofuranosyl-1,3,5-triazinane-2,4,6-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 1-pentofuranosyl-1,3,5-triazinane-2,4,6-trione(22432-96-8)
• EPA Substance Registry System: 1-pentofuranosyl-1,3,5-triazinane-2,4,6-trione(22432-96-8)

Safety Data

• Hazardous Substances Data: 22432-96-8(Hazardous Substances Data)

Usage

Molecular Structure

A complex and specific structure consisting of a pentofuranosyl group (five-carbon sugar molecule) and a triazinane-2,4,6-trione moiety (six-membered heterocyclic ring system with three nitrogen and three carbon atoms).

Triazinane-2,4,6-Trione Moiety

A six-membered heterocyclic ring system within the compound, containing three nitrogen atoms and three carbon atoms, which plays a significant role in its potential applications.

Potential Applications

Due to its unique structure and properties, 1-pentofuranosyl-1,3,5-triazinane-2,4,6-trione may have applications in various fields such as pharmaceuticals, agriculture, and materials science.

Need for Further Research

To fully understand the potential uses and effects of 1-pentofuranosyl-1,3,5-triazinane-2,4,6-trione, additional research and study are necessary.

Upstream product

• 22432-99-1 2′,3′,5′-O-tribenzoyl-1-(β-D-ribofuranosyl)cyanuric acid 
• 6974-32-9 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose 

Relevant articles and documents

Synthesis of unnatural sugar nucleotides and their evaluation as donor substrates in glycosyltransferase-catalyzed reactions

New unnatural sugar nucleotides, UDP-Fuc and CDP-Fuc were synthesized from fucose-β-1-phosphate and nucleotide monophosphates activated as morpholidates. Furthermore, a nucleotide analogue was prepared by phosphorylation of 1-(β-D-ribofuranosyl)cyanuric acid, itself obtained as a protected derivative by condensation of the persilylated derivative of cyanuric acid with 1-O-acetyl-2,3,5-tri-O-benzoyl-β-D-ribofuranose in 74% yield. This phosphate activated according to the same procedure was condensed with fucose-β-1-phosphate, affording a new sugar nucleotide conjugate (NDP-Fuc) which was evaluated together with UDP-Fuc, CDP-Fuc and ADP-Fuc, as fucose donors in α-(1→4/3)-fucosyltransferase (FucT-III) catalyzed reaction. Fucose transfer could be observed with each of the donors and kinetic parameters were determined using a fluorescent acceptor substrate. Efficiency of the four analogues towards FucT-III was in the following order: UDP-Fuc = ADP-Fuc > NDP-Fuc > CDP-Fuc. According to the same strategy ADP-GlcNAc was prepared from AMP-morpholidate and N-acetylglucosamine-α-1-phosphate; tested as a glucosaminyl donor towards Neisseria meningitidis N-acetylglucosaminyl transferase (LgtA), ADP-GlcNAc was recognized with 0.1% efficiency as compared with UDP-GlcNAc, the natural donor substrate.