3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-one (non-preferred name)

Base Information

• Chemical Name: 3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-one (non-preferred name)
• CAS No.: 5965-65-1
• Molecular Formula: C₁₂H₂₀O₁₁
• Molecular Weight: 340.284
• Mol file: 5965-65-1.mol

Synonyms:

Chemical Property of 3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-one (non-preferred name)

Chemical Property:

• Vapor Pressure: 1.06E-20mmHg at 25°C
• Boiling Point: 668.1°Cat760mmHg
• Flash Point: 252.3°C
• Density: 1.76g/cm³

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Use Description: The compound "3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-one," while having a complex and non-preferred name, serves various purposes across different fields. In the field of nutrition and dietary research, it may be studied for its potential health benefits, as it contains multiple hydroxyl groups that can contribute to antioxidant properties and overall health. 3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-one (non-preferred name) might be investigated for its role in mitigating oxidative stress and inflammation, offering insights into its use as a dietary supplement or functional food ingredient. Additionally, in the field of pharmaceuticals, it could be explored as a potential lead compound or natural product for drug development, with its unique structure suggesting therapeutic potential. While its primary significance may lie in nutrition and pharmaceutical research, its multifaceted contributions underscore its importance in advancing our understanding of health-promoting compounds and their potential applications in nutrition and medicine.

Technology Process of 3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-one (non-preferred name)

There total 9 articles about 3,4-dihydroxy-6-(hydroxymethyl)-5-{[3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl]oxy}tetrahydro-2H-pyran-2-one (non-preferred name) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 93.0%

lactobionic acid (21675-39-8) → lactobionolactone (5965-65-1,42776-28-3,52762-22-8)

Guidance literature:

In ethanol; water; at 50 ℃;

DOI:10.1002/hlca.19830660413

Reference yield: 87.0%

lactobionic acid (96-82-2,534-41-8,534-42-9,51267-45-9,58459-39-5,69728-97-8,21675-39-8) → lactobionolactone (5965-65-1,42776-28-3,52762-22-8)

Guidance literature:

lactobionic acid; In methanol; at 50 ℃; for 12h;

With trifluoroacetic acid;

DOI:10.3390/molecules26164802

Reference yield:

lactobionic acid (21675-39-8) → lactobionolactone (5965-65-1,42776-28-3,52762-22-8)

Guidance literature:

With trifluoroacetic acid; In methanol; at 65 ℃; for 8h; Temperature;

upstream raw materials:

lactobionic acid

lactobionic acid

lactobionic acid

Downstream raw materials:

lactitol

C₂₆H₃₄N₄O₁₂

6-maltobionamidocyclohexyl methacrylamide

6-maltobionamidocyclohexyl amine