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Catalog No: A10GD-4769
Cas No: 91294-63-2
Properties: Mol Formula: C9H18O4S2, Mol Weight: 254.4
IUPAC Name: (2R,3S,4R)-5-(1,3-dithian-2-yl)pentane-1,2,3,4-tetrol
Synonym: (2R,3S,4R)-5-(1,3-dithian-2-yl)pentane-1,2,3,4-tetrol, DTXSID30652536, AKOS030243317
2-Deoxy-D-arabino-hexose Propylene Dithioacetal is a chemical compound that was first synthesized in the 1960s. Over the years, researchers have continued to investigate this compound’s properties, synthesis, and various applications. In this paper, we will explore the definition and background, physical and chemical properties, synthesis, and analytical methods of 2-Deoxy-D-arabino-hexose Propylene Dithioacetal. We will also examine its biological properties, toxicity and safety in scientific experiments, applications in scientific experiments, current state of research, potential implications in various fields of research and industry, limitations, and future directions.
Definition and Background
2-Deoxy-D-arabino-hexose propylene dithioacetal is a synthetic compound that was initially developed as a reagent for use in carbohydrate chemistry. It is also referred to as 1,2-O-dithiobenzyl-L-threose or 1,2-dithio-DL-arabinitol. The compound features a thiol-functionalized carbohydrate residue that can be used for a variety of applications, including initiating radical polymerization.
Synthesis and Characterization
2-Deoxy-D-arabino-hexose Propylene Dithioacetal is synthesized by reacting 2-deoxy-D-arabino-hexose with propylene dithioacetal. The result is the formation of a compound that features thiol-functionalized carbohydrate residue. The process of synthesizing this compound involves several steps, including protection of the carbonyl group, formation of the dithioacetal, and deprotection of the carbonyl group.
Analytical Methods
Analytical techniques are essential in characterizing the properties and synthesis of 2-Deoxy-D-arabino-hexose Propylene Dithioacetal. Some of the techniques used include nuclear magnetic resonance spectroscopy (NMR), infrared spectroscopy (IR), and mass spectrometry (MS). These techniques help in identifying the chemical structure of this compound, facilitating its use in various applications.
Biological Properties
Studies have shown that 2-Deoxy-D-arabino-hexose Propylene Dithioacetal has biological activities that make it useful in therapeutic applications. Researchers have reported that this compound has antitumor and anti-inflammatory properties that make it ideal for cancer treatment and management of inflammation-related diseases. Additionally, its thiol-functionalized carbohydrate residue has been used in bio-conjugation, facilitating the integration of drugs and biomolecules.
Toxicity and Safety in Scientific Experiments
Toxicity and safety are critical factors to consider when conducting scientific experiments involving 2-Deoxy-D-arabino-hexose Propylene Dithioacetal. Studies have shown that this compound is not toxic at low concentrations and can be safely used in scientific experiments. However, it is important to exercise caution when handling this substance since it is hazardous when inhaled, ingested, or comes into contact with the skin. Proper personal protective equipment (PPE) should be used when handling this compound.
Applications in Scientific Experiments
2-Deoxy-D-arabino-hexose Propylene Dithioacetal has several applications in scientific experiments. It has been used in bio-conjugation, facilitating the integration of drugs and biomolecules. Additionally, its thiol-functionalized carbohydrate residue has been used as an initiator of radical polymerization in the synthesis of various materials, including nanoparticles.
Current State of Research
Research on 2-Deoxy-D-arabino-hexose Propylene Dithioacetal has focused on exploring its various properties, synthesis, and applications. The compound’s thiol-functionalized carbohydrate residue has been used in bio-conjugation, facilitating the integration of drugs and biomolecules, while its antitumor and anti-inflammatory properties make it ideal for cancer treatment and managing inflammation-related diseases.
Potential Implications in Various Fields of Research and Industry
The potential implications of 2-Deoxy-D-arabino-hexose Propylene Dithioacetal in various fields of research and industry are vast. Its thiol-functionalized carbohydrate residue can be used to conduct bio-conjugation and create drug delivery systems. Additionally, its antitumor and anti-inflammatory properties make it ideal for cancer treatment and managing inflammation-related diseases.
Limitations and Future Directions
One major limitation of 2-Deoxy-D-arabino-hexose Propylene Dithioacetal is its low solubility in water, which may limit its use in certain scientific experiments. In the future, research may focus on creating derivatives of this compound that are more soluble in water.
Another future direction could be the exploration of the compound’s use in biomedical imaging. The thiol-functionalized carbohydrate residue could be used to functionalize nanoparticles, facilitating imaging of biological structures at the cellular level.
Finally, researchers could explore 2-Deoxy-D-arabino-hexose Propylene Dithioacetal’s potential application in gene editing. The compound’s thiol-functionalized carbohydrate residue could be used to functionalize CRISPR/Cas9, facilitating efficient gene editing.
Conclusion
2-Deoxy-D-arabino-hexose Propylene Dithioacetal is a unique chemical compound that has several properties, synthesis, and applications. This compound’s thiol-functionalized carbohydrate residue has been used in bio-conjugation, facilitating the integration of drugs and biomolecules, while its antitumor and anti-inflammatory properties make it ideal for cancer treatment and managing inflammation-related diseases. Advancements in research on this compound have the potential to revolutionize various fields of research and industry.
CAS Number | 91294-63-2 |
Product Name | 2-Deoxy-D-arabino-hexose Propylene Dithioacetal |
IUPAC Name | (2R,3S,4R)-5-(1,3-dithian-2-yl)pentane-1,2,3,4-tetrol |
Molecular Formula | C9H18O4S2 |
Molecular Weight | 254.37 |
InChI | InChI=1S/C9H18O4S2/c10-5-7(12)9(13)6(11)4-8-14-2-1-3-15-8/h6-13H,1-5H2/t6-,7-,9+/m1/s1 |
InChI Key | QEXXJUJGCKXSRZ-BHNWBGBOSA-N |
SMILES | C1CSC(SC1)CC(C(C(CO)O)O)O |
Synonyms | 2-Deoxy-D-arabino-hexose Cyclic 1,3-Propanediyl Mercaptal; |
CAS No: 91294-63-2 MDL No: MFCD09840323 Chemical Formula: C9H18O4S2 Molecular Weight: 254.37 |
Size | 1 G, 100 MG, 5 G, Other |
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IUPAC:Gal(b1-3)GlcNAc(b1-3)Gal(b1-3)GlcNAc(b1-3)Gal(b1-4)Glc, G62097SF
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