4258-01-9

Basic information

• Product Name: 2-Deoxy-β-D-erythro-pentopyranose Triacetate
• Synonyms: 2-Deoxy-D-ribose 1,3,4-Triacetate;2-Deoxy-β-D-erythro-pentopyranose Triacetate;β-D-2-Deoxy-ribopyranose Triacetate;[(2S,4S,5R)-2,5-diacetyloxyoxan-4-yl] acetate
• CAS NO: 4258-01-9
• Molecular Formula: C₁₁H₁₆O₇
• Molecular Weight: 260.24054
• Product Categories: Carbohydrates & Derivatives
• Mol File: 4258-01-9.mol

Chemical Properties

• Appearance: /
• Storage Temp.: Refrigerator
• Solubility: Chloroform, Toluene
• CAS DataBase Reference: 2-Deoxy-β-D-erythro-pentopyranose Triacetate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Deoxy-β-D-erythro-pentopyranose Triacetate(4258-01-9)
• EPA Substance Registry System: 2-Deoxy-β-D-erythro-pentopyranose Triacetate(4258-01-9)

Safety Data

• Hazardous Substances Data: 4258-01-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
2-Deoxy-β-D-erythro-pentopyranose Triacetate is used as a pharmaceutical compound for its ability to induce apoptosis in cells. This is achieved by inhibiting the synthesis of glutathione, an essential antioxidant, and increasing its efflux, leading to cell death. This property makes it a promising candidate for the development of drugs targeting various diseases, particularly those involving uncontrolled cell growth.
Used in Chemical Research:
As a white solid with distinct chemical properties, 2-Deoxy-β-D-erythro-pentopyranose Triacetate can be utilized in chemical research for the synthesis of other complex molecules or as a starting material for the development of novel compounds with potential applications in various industries.
Used in Biochemical Studies:
The unique structure of 2-Deoxy-β-D-erythro-pentopyranose Triacetate allows it to be used in biochemical studies, particularly in understanding the role of sugar molecules in biological processes. It can be employed as a tool to investigate the interactions between sugar molecules and proteins, enzymes, or other biomolecules, contributing to the advancement of our knowledge in biochemistry and molecular biology.

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