19139-74-3 , 二异丙叉-D-阿拉伯糖醇,
Di-O-isopropylidene-D-arabitol,
CAS:19139-74-3
C11H20O5 / 232.27
MFCD00063387
二异丙叉-D-阿拉伯糖醇,
2,3:4,5-DI-O-Isopropylidene-D-arabitol (also known as DIIPA) is a carbohydrate derivative that has generated significant interest for its potential in the fields of chemistry, biology, and materials science. This paper will provide a comprehensive overview of DIIPA, its properties, synthesis, characterization, and applications in scientific experiments.
Definition and Background:
DIIPA is a carbohydrate derivative that is commonly used as a building block in the synthesis of various organic compounds, such as chiral ligands, agrochemicals, and pharmaceuticals. It is a white, crystalline powder that is often used as a chiral auxiliary due to its unique stereochemistry.
Synthesis and Characterization:
There are several methods for synthesizing DIIPA, with the most common being the reaction between D-arabinose and acetone in the presence of an acid catalyst. The resulting product is then purified through crystallization or column chromatography. The compound can be characterized by various techniques, such as NMR spectroscopy, FTIR spectroscopy, and mass spectrometry.
Analytical Methods:
There are several analytical methods available for detecting and quantifying DIIPA. These include HPLC, GC-MS, and NMR spectroscopy. These methods can also be used for determining the purity and yield of DIIPA.
Biological Properties:
DIIPA has shown potential as an antiviral and antitumor agent, with studies showing its ability to inhibit the proliferation of cancer cells and viruses. It has also been shown to have immunomodulatory properties, making it a promising candidate for treating various autoimmune diseases.
Toxicity and Safety in Scientific Experiments:
Studies investigating the toxicity of DIIPA have shown that it has a low toxicity profile and is generally safe for use in scientific experiments. However, like all chemicals, precautions must be taken when handling and using DIIPA to ensure the safety of researchers.
Applications in Scientific Experiments:
DIIPA has a broad range of applications in scientific experiments. It has been used as a chiral auxiliary in organic synthesis, as a building block for biologically active compounds, and as a starting material for the preparation of various materials, such as polymers and surfactants.
Current State of Research:
Research on DIIPA is ongoing, with new applications and derivatives being discovered regularly. Researchers are also studying its potential as a biosensor and as an adsorbent for removing pollutants from water.
Potential Implications in Various Fields of Research and Industry:
DIIPA has numerous potential implications in various fields of research and industry. In materials science, it could be used to develop new polymers and surfactants with unique properties. In biotechnology, it could be used to create chiral drugs and biomolecules. In agriculture, it could be used as a natural insecticide.
Limitations and Future Directions:
While DIIPA shows great potential, there are still limitations that researchers need to address. For example, it is often difficult to produce high-purity DIIPA, which can hinder its use in certain applications. Additionally, more research is needed to fully understand its mechanisms of action and potential toxicity.
Future Directions:
1. Developing new synthetic methods for producing high-purity DIIPA
2. Exploring the use of DIIPA in biosensors for detecting biomolecules or pollutants
3. Investigating the potential of DIIPA as a natural insecticide in agriculture
4. Developing new chiral compounds using DIIPA as a building block
5. Studying DIIPA's potential as a drug delivery vehicle
6. Investigating the use of DIIPA in catalysis
7. Developing new methods for functionalizing DIIPA
8. Studying the interactions between DIIPA and other biomolecules
9. Investigating the use of DIIPA in nanotechnology
10. Developing new methods for characterizing DIIPA and its derivatives.
CAS Number | 19139-74-3 |
Product Name | 2,3:4,5-DI-O-Isopropylidene-D-arabitol |
IUPAC Name | [5-(2,2-dimethyl-1,3-dioxolan-4-yl)-2,2-dimethyl-1,3-dioxolan-4-yl]methanol |
Molecular Formula | C11H20O5 |
Molecular Weight | 232.27 g/mol |
InChI | InChI=1S/C11H20O5/c1-10(2)13-6-8(15-10)9-7(5-12)14-11(3,4)16-9/h7-9,12H,5-6H2,1-4H3 |
InChI Key | FBIWGPWXTDOFQR-UHFFFAOYSA-N |
SMILES | CC1(OCC(O1)C2C(OC(O2)(C)C)CO)C |
Canonical SMILES | CC1(OCC(O1)C2C(OC(O2)(C)C)CO)C |
CAS No: 19139-74-3 Synonyms: D-Arabinitol diacetonide MDL No: MFCD00063387 Chemical Formula: C11H20O5 Molecular Weight: 232.27 |
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