1, 3, 5-Tri-O-acetyl-2-deoxy-D-ribose, CAS:4594-52-9

1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose is a monosaccharide that belongs to the class of deoxy sugars that are lacking a hydroxyl group. This type of sugar is present in DNA in the form of deoxyribose. This chemical compound is an important building block in the synthesis of various biologically relevant molecules. It is used in the development of nucleic acid analogs, glycopeptides, glycolipids, and other biologically active compounds. Synthesis and Characterization: 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose can be synthesized from D-ribose by treatments with acetic anhydride, pyridine, and sodium acetate. The compound can be characterized using various analytical techniques such as mass spectrometry, infrared (IR) spectroscopy, and nuclear magnetic resonance (NMR) spectroscopy. Analytical Methods: 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose can be quantified using high-performance liquid chromatography (HPLC) techniques. It can be detected by using various detection modes such as UV, fluorescence, and electrochemical detection. The sugar derivative can also be analyzed using mass spectrometry and NMR spectroscopy techniques. Biological Properties: 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose exhibits a broad range of biological properties. It has been shown to exhibit anti-cancer, anti-inflammatory, and anti-viral properties. It is also widely used in the development of glycoconjugate vaccines, where it acts as a potent immunogen. Toxicity and Safety in Scientific Experiments: 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose is generally safe for use in scientific experiments. However, like any other chemical compound, it can be toxic if not handled properly. It is important to follow safety procedures while handling this compound. Applications in Scientific Experiments: 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose has a wide range of applications in scientific experiments. It is used in the synthesis of various biologically active molecules such as nucleosides, nucleotides, and glycoconjugates. It is also widely used in the development of glycopeptide and glycolipids. Current State of Research: Research on 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose is ongoing in various fields such as organic chemistry, biochemistry, and pharmaceutical sciences. The compound is currently being investigated as an important building block in the development of various biologically active compounds. Potential Implications in Various Fields of Research and Industry: 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose has potential implications in various fields of research and industry. It can be used in the development of new drugs, vaccines, and other biologically active compounds. The compound can also be used in the development of materials with unique properties such as hydrogels and nanomaterials. Limitations and Future Directions: Although 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose has numerous potential applications, it has some limitations. The synthesis of this sugar derivative can be expensive and time-consuming. Further research is needed to develop more efficient synthesis protocols. Additionally, more research is needed to explore the full potential of this chemical compound in various fields of research and industry. Future Directions: 1. Developing more efficient synthesis techniques 2. Studying the structure-activity relationship of 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose derivatives 3. Developing 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose-based hydrogels for biomedical applications 4. Studying the potential use of 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose derivatives as anti-viral agents 5. Developing new glycoconjugate vaccines using 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose derivatives 6. Studying the potential use of 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose derivatives in cosmetic applications 7. Developing 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose-based sensors for environmental monitoring 8. Studying the pharmacokinetics and pharmacodynamics of 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose-based drugs 9. Developing new methodologies for the detection and quantification of 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose derivatives in biological samples. 10. Exploring the use of 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose derivatives in nanomaterials. CAS Number 4594-52-9 Product Name 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose IUPAC Name [(2R,3S)-3,5-diacetyloxyoxolan-2-yl]methyl acetate Molecular Formula C11H16O7 Molecular Weight 260.24 g/mol InChI InChI=1S/C11H16O7/c1-6(12)15-5-10-9(16-7(2)13)4-11(18-10)17-8(3)14/h9-11H,4-5H2,1-3H3/t9-,10+,11?/m0/s1 InChI Key QAGMBTAACMQRSS-MTULOOOASA-N SMILES CC(=O)OCC1C(CC(O1)OC(=O)C)OC(=O)C Synonyms 2-Deoxy-D-erythro-pentofuranose 1,3,5-Triacetate; 2-Deoxy-D-erythro-pentofuranose Triacetate; 2-Deoxyribose 1,3,5-Triacetate; 2-Deoxy-D-ribose 1,3,5-Triacetate; 1,3,5-Tri-O-acetyl-2-deoxy-D-erythro-pentofuranose; 1,3,5-Tri-O-acetyl-2-deoxy-D-ribofura Canonical SMILES CC(=O)OCC1C(CC(O1)OC(=O)C)OC(=O)C Isomeric SMILES CC(=O)OC[C@@H]1[C@H](CC(O1)OC(=O)C)OC(=O)C CAS No: 4594-52-9 MDL No: MFCD08458437 Chemical Formula: C11H16O7 Molecular Weight: 260.24 In Stock.?? COA: Product name:  1,3,5-Tri-O-acetyl-2-deoxy-D-ribose                        CAS:  4594-52-9 M.F. : C 11 H 16 O 7              M .W. :  260.24        Batch No : 20120415      Quantity :50g from 102.3g Items Standards Results Appearance Yellowish syrup Positive Solubility Soluble in CHCl 3  and insoluble in H 2 O Complies Appearance of solution Dissolve0.5 gin 10 ml of CHCl 3 , and the solution should be clear Complies NMR and ESI-MS Should comply Complies Identification IR and TLC Positive Residue on ignition Max. 0.5% 0.05% Heavy metal Max. 50ppm Complies TLC   (15%H 2 SO 4 -C 2 H 5 OH) Should be one or two spots Complies Assay  ? alpha and Beta ? Min.98% Complies