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  • 138892-04-3, 1-脱氧-1-叠氮-alpha-D-阿拉伯糖 ,a-D-Arabinopyranosyl azide, CAS:138892-04-3
138892-04-3, 1-脱氧-1-叠氮-alpha-D-阿拉伯糖 ,a-D-Arabinopyranosyl azide, CAS:138892-04-3

138892-04-3, 1-脱氧-1-叠氮-alpha-D-阿拉伯糖 ,a-D-Arabinopyranosyl azide, CAS:138892-04-3

138892-04-3 ,a-D-Arabinopyranosyl azide,
1-脱氧-1-叠氮-alpha-D-阿拉伯糖,
CAS:138892-04-3
C5H9N3O4 / 175.144
MFCD09750686

a-D-Arabinopyranosyl azide

1-脱氧-1-叠氮-alpha-D-阿拉伯糖

Alpha-D-arabinopyranosyl azide, also known as α-L-arabinofuranosyl azide, is a sugar-based compound. It is a widely used chemical in scientific research and has emerged as an important compound in various fields of research and industry. In this review, we aim to analyze the definition, background, physical and chemical properties, synthesis and characterization, analytical methods, 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 of alpha-D-arabinopyranosyl azide.

Definition and Background:

Alpha-D-arabinopyranosyl azide is a sugar-based compound that is made of an azido group (--N3) and a sugar ring. It is a highly reactive compound and is widely used as a precursor for the synthesis of various bioactive compounds. It has proven to be a valuable compound in the synthesis of nucleoside analogues, glycosylation reagents, and biologically active molecules.

Physical and Chemical Properties:

Alpha-D-arabinopyranosyl azide is a crystalline solid with a white to off-white color. It has a molecular formula of C5H9N3O4 and a molecular weight of 175.144 g/mol. It is soluble in water, methanol, and ethanol. The compound is sensitive to heat and shock and is highly explosive.

Synthesis and Characterization:

The synthesis of alpha-D-arabinopyranosyl azide can be achieved by different methods. The most commonly used method involves the reaction of arabinose with sodium azide in the presence of triethylamine. The compound can also be synthesized by the reaction of arabinose with tetraethylammonium azide or by the direct conversion of alpha-D-arabinopyranosyl bromide to alpha-D-arabinopyranosyl azide.

Analytical Methods:

The purity and identity of alpha-D-arabinopyranosyl azide can be determined by various analytical methods. These methods include thin-layer chromatography, high-performance liquid chromatography, and nuclear magnetic resonance spectroscopy. The purity of the compound can also be determined by measuring the melting point of the compound.

Biological Properties:

Alpha-D-arabinopyranosyl azide has been found to exhibit various biological properties. It is an important precursor for the synthesis of nucleoside analogues that are widely used as antiviral and anticancer agents. It has also been found to possess anti-inflammatory, antitumor, and antibacterial properties.

Toxicity and Safety in Scientific Experiments:

Alpha-D-arabinopyranosyl azide is a highly reactive compound and should be handled with care. It is highly explosive and can pose a hazard if not handled properly. In scientific experiments, it should be handled under controlled conditions and by trained personnel.

Applications in Scientific Experiments:

Alpha-D-arabinopyranosyl azide is a valuable compound in scientific research. It is widely used in the synthesis of nucleoside analogues, glycosylation reagents, and biologically active molecules. In addition, it has been used as a precursor for the synthesis of radiolabeled compounds for imaging studies.

Current State of Research:

The research on alpha-D-arabinopyranosyl azide is ongoing. New methods for the synthesis of the compound are being developed, and its potential in the synthesis of bioactive molecules is being explored. Moreover, its use in imaging studies is gaining attention.

Potential Implications in Various Fields of Research and Industry:

Alpha-D-arabinopyranosyl azide has potential implications in various fields of research and industry. It can be used in the synthesis of nucleoside analogues, glycosylation reagents, and biologically active molecules. Moreover, its use in imaging studies can contribute to the development of new diagnostic tools for various diseases.

Limitations and Future Directions:

One of the limitations of alpha-D-arabinopyranosyl azide is its sensitivity to heat and shock. This limits its usage in certain experimental conditions. Furthermore, additional research is needed to further explore its potential in various fields of research and industry.

Future Directions:

In the future, research on alpha-D-arabinopyranosyl azide should focus on:

1. Developing new methods for the synthesis of the compound that are more efficient and cost-effective.

2. Exploring its potential in the development of new diagnostic tools for various diseases.

3. Developing safer and more reliable methods for handling and storing the compound.

4. Further exploring its applications in the synthesis of bioactive molecules and its use in imaging studies.

Conclusion:

Alpha-D-arabinopyranosyl azide is a valuable compound in scientific research. Its potential applications in the synthesis of bioactive molecules and in imaging studies make it an important compound in various fields of research and industry. However, its sensitivity to heat and shock and the need for handling it under controlled conditions limit its usage in certain experimental conditions. Further research is needed to explore its potential in various fields of research and industry.

CAS Number138892-04-3
Product Namealpha-D-Arabinopyranosyl azide
IUPAC Name(2S,3S,4R,5R)-2-azidooxane-3,4,5-triol
Molecular FormulaC5H9N3O4
Molecular Weight175.144
InChIInChI=1S/C5H9N3O4/c6-8-7-5-4(11)3(10)2(9)1-12-5/h2-5,9-11H,1H2/t2-,3-,4+,5+/m1/s1
InChI KeyWVWBURHISBVZHI-MBMOQRBOSA-N
SMILESC1C(C(C(C(O1)N=[N+]=[N-])O)O)O
CAS No: 138892-04-3 MDL No: MFCD09750686 Chemical Formula: C5H9N3O4 Molecular Weight: 175.144
References: 1. Dinya Z, Benke P, Györgydeák Z, et al., J. Mass Spectrom. Vol36, No2, p211-219

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