157024-67-4

Basic information

• Product Name: β-Glucosylglycerol 2,3,4,6-Tetraacetate
• Synonyms: β-Glucosylglycerol 2,3,4,6-Tetraacetate;2-(Tetraacetylglucosido)glycerol;2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl Glycerol;2-Hydroxy-1-(hydroxyMethyl)ethyl β-D-Glucopyranoside 2,3,4,6-Tetraacetate
• CAS NO: 157024-67-4
• Molecular Formula: C₁₇H₂₆O₁₂
• Molecular Weight: 422.38114
• Product Categories: Carbohydrates & Derivatives;Intermediates;Carbohydrates & Derivatives, Intermediates
• Mol File: 157024-67-4.mol

Chemical Properties

• Melting Point: 103 °C
• Boiling Point: 527.2±50.0 °C(Predicted)
• Appearance: /
• Density: 1.35±0.1 g/cm3(Predicted)
• Solubility: Chloroform, Dichloromethane, Ethanol, Ethyl Acetate, Methanol,
• PKA: 13.83±0.10(Predicted)
• CAS DataBase Reference: β-Glucosylglycerol 2,3,4,6-Tetraacetate(CAS DataBase Reference)
• NIST Chemistry Reference: β-Glucosylglycerol 2,3,4,6-Tetraacetate(157024-67-4)
• EPA Substance Registry System: β-Glucosylglycerol 2,3,4,6-Tetraacetate(157024-67-4)

Safety Data

• Hazardous Substances Data: 157024-67-4(Hazardous Substances Data)

Usage

Uses

Used in Chemical Synthesis:
β-Glucosylglycerol 2,3,4,6-Tetraacetate is used as an intermediate in the synthesis of β-Glucosylglycerol for the development of various chemical products. Its role as a protected intermediate allows for the controlled formation of the desired compound, ensuring the successful synthesis of the final product.
Used in Pharmaceutical Industry:
β-Glucosylglycerol 2,3,4,6-Tetraacetate is used as a building block in the creation of pharmaceutical compounds. Its unique chemical structure contributes to the development of new drugs with potential therapeutic applications.
Used in Cosmetics Industry:
In the cosmetics industry, β-Glucosylglycerol 2,3,4,6-Tetraacetate is used as an ingredient in the formulation of skincare and beauty products. Its properties may contribute to the development of products with enhanced moisturizing, emollient, or protective qualities.
Used in Research and Development:
β-Glucosylglycerol 2,3,4,6-Tetraacetate is utilized in research and development for the study of its chemical properties and potential applications in various fields. Its role as a protected intermediate and building block allows scientists to explore its potential in creating new compounds and materials.

Upstream product

• 604-69-3 β-D-glucose pentaacetate 
• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 
• 76222-76-9 (ξ-2-phenyl-[1,3]dioxan-5-yl)-[tetra-O-acetyl-β-D-glucopyranoside 
• 157024-66-3 1,3-di-O-benzyl-2-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-sn-glycerol 

Downstream Products

• 534-68-9 2-O-β-D-glucosyl-glycerol 

Relevant articles and documents

Synthesis of glycosyl glycerols and related glycolipids

Several isomeric glycosyl glycerols were synthesized. Acetylated allyl glycosides of D-glucose and D-galactose were transformed into 1-O-(glycopyranosyl)-rac-glycerols in a three step procedure via the corresponding 2,3-epoxypropyl glycosides and the peracetylated glycosyl glycerols. Tetra-O-benzyl-D-glucose was glycosylated with 1,3-di-O-benzylglycerol to give the α-anomer preferentially. The 2-O-(tetra-O-acetyl-β-glycopyranosyl)-sn-glycerols and 2-O-(β-glycopyranosyl)-sn-glycerols of D-glucose, D-galactose and N-acetyl-D-glucosamine and the corresponding α-derivatives of D-mannose were synthesized by selective glycosylation methods from 1,3-di-O-benzylglycerol and 1,3-O-benzylideneglycerol, respectively, and activated sugar compounds followed by hydrogenolysis. After long chain acylation and selective deacetylation the 1,3-di-O-acyl-2-O-β-glycopyranosyl)-sn-glycerols of D-glucose, D-galactose and N-acetyl-D-glucosamine and the corresponding α-derivative of D-mannose were synthesized.