Cas no 30571-56-3 (1,2,3,5-Tetra-O-acetyl-D-xylofuranose)

1,2,3,5-Tetra-O-acetyl-D-xylofuranose structure
30571-56-3 structure
Product Name:1,2,3,5-Tetra-O-acetyl-D-xylofuranose
CAS No:30571-56-3
MF:C13H18O9
MW:318.276625156403
MDL:MFCD27986490
CID:316085
PubChem ID:11162923
Update Time:2025-04-24

1,2,3,5-Tetra-O-acetyl-D-xylofuranose Chemical and Physical Properties

Names and Identifiers

    • D-Xylose,2,3,4,5-tetraacetate
    • (2,3,4-triacetyloxy-5-oxopentyl) acetate
    • 1,2,3,5-TETRA-O-ACETYL-D- XYLOFURANOSE
    • 2,3,4,5-tetra-O-acetyl-aldehydo-D-xylose
    • 2,3,4,5-tetra-O-acetyl-D-xylose
    • D-xylose tetraacetate
    • SYRUP
    • Tetra-O-acetyl-aldehydo-D-xylose
    • tetra-O-acetyl-D-xylose
    • xylose tetraacetate
    • D-Xylofuranose, 1,2,3,5-tetraacetate
    • PD017536
    • 1,2,3,5-Tetraacetate D-xylofuranose
    • FT-0772938
    • 42927-46-8
    • [(2R,3S,4R)-3,4,5-triacetyloxyoxolan-2-yl]methyl acetate
    • AKOS027430446
    • CS-0226672
    • 1H-Pyrrole-2-carboxylic acid, 3,4-dimethyl-
    • (3R,4S,5R)-5-(Acetoxymethyl)tetrahydrofuran-2,3,4-triyl triacetate
    • IHNHAHWGVLXCCI-DAAZQVBGSA-N
    • xylo-furanose tetraacetate
    • SCHEMBL338322
    • 30571-56-3
    • W-202260
    • 1,2,3,5-tetra-O-acetyl-D-xylofuranose
    • 1,2,3,5-Tetra-O-acetyl-D-xylofuranose
    • MDL: MFCD27986490
    • Inchi: 1S/C13H18O9/c1-6(14)18-5-10-11(19-7(2)15)12(20-8(3)16)13(22-10)21-9(4)17/h10-13H,5H2,1-4H3/t10-,11+,12-,13?/m1/s1
    • InChI Key: IHNHAHWGVLXCCI-DAAZQVBGSA-N
    • SMILES: O1C([C@@H]([C@H]([C@H]1COC(C)=O)OC(C)=O)OC(C)=O)OC(C)=O

Computed Properties

  • Exact Mass: 318.09504
  • Monoisotopic Mass: 318.095
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 9
  • Heavy Atom Count: 22
  • Rotatable Bond Count: 9
  • Complexity: 458
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 3
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.7
  • Topological Polar Surface Area: 114A^2

Experimental Properties

  • Density: 1.245g/cm3
  • Melting Point: 90 - 91 °C (乙醚)
  • Boiling Point: 410.2oC at 760 mmHg
  • Flash Point: 180oC
  • Refractive Index: 1.455
  • PSA: 122.27
  • LogP: -0.45650

1,2,3,5-Tetra-O-acetyl-D-xylofuranose Pricemore >>

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1,2,3,5-Tetra-O-acetyl-D-xylofuranose Related Literature

Additional information on 1,2,3,5-Tetra-O-acetyl-D-xylofuranose

D-Xylose, 2,3,4,5-Tetraacetate: A Comprehensive Overview

D-Xylose, 2,3,4,5-Tetraacetate, also known by its CAS number 30571-56-3, is a derivative of D-xylose that has gained significant attention in various scientific and industrial applications. This compound is a fully acetylated form of D-xylose, where the hydroxyl groups at positions 2, 3, 4, and 5 are replaced by acetyl groups. The structural modification enhances its stability and functionality, making it a valuable compound in fields such as biochemistry, pharmacology, and material science.

The synthesis of D-Xylose, 2,3,4,5-Tetraacetate typically involves the acetylation of D-xylose using acetylating agents such as acetic anhydride in the presence of a catalyst. This process ensures the complete protection of the hydroxyl groups on the sugar molecule. The resulting compound is a white crystalline solid with a molecular formula of C11H18O8 and a molecular weight of 286.26 g/mol.

One of the most notable applications of D-Xylose, 2,3,4,5-Tetraacetate is in the field of glycobiology. It serves as a useful precursor for the synthesis of various glycoconjugates and glycolipids. The acetylated form allows for easier manipulation and modification of the sugar structure without interference from hydroxyl groups. Recent studies have highlighted its role in the development of novel therapeutic agents targeting carbohydrate-based receptors.

In addition to its biochemical applications, D-Xylose derivatives have found utility in the food industry as stabilizers and texturizing agents. The tetraacetate form is particularly valued for its ability to enhance the shelf life of food products while maintaining their sensory properties. Researchers have explored its potential as a natural alternative to synthetic stabilizers in processed foods.

The pharmaceutical industry has also benefited from the unique properties of D-Xylose derivatives. The tetraacetate form is used as an intermediate in drug delivery systems due to its ability to modulate drug release kinetics. Recent advancements have focused on its application in targeted drug delivery systems where controlled release is critical for therapeutic efficacy.

From an environmental perspective, D-Xylose derivatives are being investigated for their potential in biodegradable materials. The tetraacetate form can be incorporated into polymers to enhance their biocompatibility and degradation profiles. This aligns with current trends toward sustainable materials development.

In terms of safety, D-Xylose, including its tetraacetate derivative,is generally considered safe for consumption when used at recommended levels. However,pregnant women or individuals with specific health conditions should consult healthcare professionals before incorporating it into their diet.

In conclusion,D-Xylose, particularly its fully acetylated form (D-Xylose,2,3,4,5-tetraacetate) continues to be a versatile compound with expanding applications across multiple disciplines. Its unique chemical properties make it an invaluable tool for researchers and industry professionals alike.

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