Cas no 37076-71-4 ((3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate)

(3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate is a chiral carbohydrate derivative characterized by its stereospecific triacetate functionalization on a methyl-substituted tetrahydrofuran backbone. Its defined (3R,4R,5R) configuration ensures high enantiomeric purity, making it valuable for asymmetric synthesis and pharmaceutical intermediates. The acetyl groups enhance stability and solubility in organic solvents, facilitating its use in glycosylation reactions and nucleoside chemistry. This compound is particularly useful in the synthesis of complex natural products and modified sugars, where precise stereocontrol is critical. Its well-defined structure and reactivity profile make it a reliable building block for research in medicinal chemistry and carbohydrate-based materials.
(3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate structure
37076-71-4 structure
Product Name:(3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate
CAS No:37076-71-4
MF:C11H16O7
MW:260.240544319153
CID:319456
PubChem ID:11196237
Update Time:2025-10-24

(3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate Chemical and Physical Properties

Names and Identifiers

    • (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate
    • 1,2,3-Triacety1-5-deoxy-beta-D-ribofuranose
    • 5-DEOXY-1,2,3-TRI-O-ACETYL-B-D-RIBOFURANOSIDE
    • D-Ribofuranose,5-deoxy-, triacetate (9CI)
    • 1,2,3-Tri-O-acetyl-5-deoxy-D-ribofuranose
    • 1,2,3-Tri-O-acetyl-5-deoxyribofuranose
    • 5-deoxy-1,2,3-tri-O-acetyl-D-ribofuranose
    • 5-Deoxy-D-ribofuranose triacetate
    • 5-deoxy-D-ribose-1,2,3-tri-O-acetate
    • 5'-deoxyribofuranose 1,2,3-triacetate
    • 5-desoxy-1,2,3-tri-O-acetyl-D-ribofuranose
    • tri-O-acetyl-5-deoxy-D-ribofuranose
    • 1,2,3-tri-O-acetyl-5-deoxy-ribofuranose
    • AKOS025214001
    • CS-0089030
    • 1,2,3-tri-O-acetyl-5deoxy-D-ribofuranose
    • EINECS 253-335-1
    • W-110887
    • (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyltriacetate
    • 37076-71-4
    • [(2R,3R,4R)-4,5-diacetyloxy-2-methyloxolan-3-yl] acetate
    • NXEJETQVUQAKTO-ZBCCYFLUSA-N
    • NS00088271
    • SCHEMBL332549
    • MDL： MFCD09038578
    • Inchi： 1S/C11H16O7/c1-5-9(16-6(2)12)10(17-7(3)13)11(15-5)18-8(4)14/h5,9-11H,1-4H3/t5-,9-,10-,11?/m1/s1
    • InChI Key： NXEJETQVUQAKTO-ZBCCYFLUSA-N
    • SMILES： O1C([C@@H]([C@@H]([C@H]1C)OC(C)=O)OC(C)=O)OC(C)=O

Computed Properties

  • Exact Mass: 260.08958
  • Monoisotopic Mass: 260.08960285g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 18
  • Rotatable Bond Count: 6
  • Complexity: 351
  • 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: 0.3
  • Topological Polar Surface Area: 88.1?2

Experimental Properties

  • PSA: 88.13

(3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate Pricemore >>

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(3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate Suppliers

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(CAS:37076-71-4)Tri-O-acetyl-5-deoxy-D-ribofuranose
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Quantity:10g
Purity:97%
Pricing Information Last Updated:Friday, 18 July 2025 16:06
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(3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate Related Literature

Additional information on (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate

CAS No 37076-71-4: (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate

The compound (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate with CAS No 37076-71-4 is a highly specialized organic molecule that has garnered significant attention in the fields of organic chemistry and pharmacology. This compound is notable for its unique stereochemistry and functional group arrangement, which contribute to its versatile applications in both academic research and industrial settings.

Tetrahydrofuran (THF) derivatives have long been recognized for their utility as solvents and intermediates in organic synthesis. However, the triacetate derivative of this compound adds an additional layer of complexity and functionality. The triacetate groups introduce ester functionalities that can participate in various chemical reactions, making this compound a valuable building block in the synthesis of more complex molecules.

Recent studies have highlighted the potential of (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate in the development of novel drug delivery systems. Its ability to form stable complexes with various bioactive molecules has been exploited in the creation of targeted drug delivery vehicles. Researchers have demonstrated that the compound's stereochemistry plays a crucial role in determining its compatibility with biological systems.

In addition to its pharmacological applications, this compound has found use in the synthesis of advanced materials. The triacetate groups facilitate the formation of cross-linked networks when subjected to specific reaction conditions. These networks exhibit unique mechanical properties that make them suitable for applications in polymer science and materials engineering.

The synthesis of (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate involves a multi-step process that requires precise control over stereochemistry. Recent advancements in asymmetric catalysis have enabled the efficient production of this compound with high enantiomeric purity. This development has significantly enhanced its utility in chiral recognition studies and enantioselective reactions.

Furthermore, the compound's role as a precursor in the synthesis of bioactive molecules has been extensively explored. Its ability to undergo various transformations while retaining its stereochemical integrity makes it an invaluable tool in medicinal chemistry. Researchers have successfully utilized this compound to synthesize analogs of natural products with potent biological activities.

Recent research has also focused on the environmental impact of (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate and its degradation pathways. Studies indicate that under specific conditions, the compound can undergo biodegradation without releasing harmful byproducts. This finding is particularly important for its application in sustainable chemical processes.

In conclusion,CAS No 37076-71-4, or (3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate, stands as a testament to the ingenuity of modern organic chemistry. Its diverse applications and promising research outcomes underscore its importance as a key molecule in both academic and industrial contexts.

37076-71-4 ((3R,4R,5R)-5-Methyltetrahydrofuran-2,3,4-triyl triacetate) Related Products

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NewCan Biotech Limited
(CAS:37076-71-4)Tri-O-acetyl-5-deoxy-D-ribofuranose
NC15840
Purity:97%
Quantity:10g
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