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  • 101833-22-1, 乙基-4,6-O-苄叉-b-D-吡喃半乳糖苷, CAS:101833-22-1
101833-22-1, 乙基-4,6-O-苄叉-b-D-吡喃半乳糖苷, CAS:101833-22-1

101833-22-1, 乙基-4,6-O-苄叉-b-D-吡喃半乳糖苷, CAS:101833-22-1

101833-22-1 , 乙基-4,6-O-苄叉-beta-D-吡喃半乳糖苷,
Ethyl 4,6-O-benzylidene-b-D-galactopyranoside,
CAS:101833-22-1
C15H20O6 /296.32
MFCD07367505

Ethyl 4,6-O-benzylidene-b-D-galactopyranoside

乙基-4,6-O-苄叉-beta-D-吡喃半乳糖苷,

Ethyl 4,6-O-benzylidene-β-D-galactopyranoside is a carbohydrate that belongs to the monosaccharide class. It is glycosylated with an ethyl group at the hydroxyl group at the 6th position and methylated on the benzene ring at the 4th position. This modification has been shown to increase its solubility in water and its stability in basic solutions. The synthesis of this compound is performed through a click reaction, which allows for high purity and custom synthesis. Ethyl 4,6-O-benzylidene-β-D-galactopyranoside can be used as a sugar substitute or in pharmaceuticals for treatment of diabetes mellitus type 2.

Ethyl 4,6-O-benzylidene-b-D-galactopyranoside, also known as EBGP, is a compound that belongs to the group of benzylidene derivatives of carbohydrates. It is a colorless powder that has a sweet odor. EBGP is of great interest to researchers due to its unique properties and potential applications in various fields of research and industry.

Synthesis and Characterization:

EBGP can be synthesized through a reaction between galactose and benzaldehyde in the presence of strong acid catalysts, such as hydrochloric acid. The reaction yields the crystalline product that can be purified through recrystallization.

The characterization of EBGP is done using different analytical techniques such as nuclear magnetic resonance spectroscopy, mass spectrometry, and infrared spectroscopy.

Analytical Methods:

Nuclear Magnetic Resonance (NMR) spectroscopy is an analytical technique that is frequently used to characterize EBGP. The technique is based on the interaction of electromagnetic radiation with the nuclear spins of atoms. Infrared spectroscopy is another analytical technique used to determine the functional groups present in EBGP. The technique is based on the absorption of infrared radiation by the functional groups present in the compound.

Biological Properties:

EBGP has been shown to have potential applications in various fields due to its biological properties. Studies have demonstrated that EBGP can inhibit the growth of cancer cells by inducing apoptosis. EBGP displays promising antimicrobial activity against Gram-positive bacteria which makes it a potential source of antibiotics.

Toxicity and Safety in Scientific Experiments:

EBGP is considered to be relatively safe and non-toxic in scientific experiments, as no severe adverse effects or fatalities have been reported in the available literature. However, like any chemical compound, proper handling and disposal procedures must be followed.

Applications in Scientific Experiments:

EBGP has potential applications as building blocks in organic synthesis and as a starting material for the preparation of other benzylidene derivatives of carbohydrates. EBGP also has potential applications for the development of novel drugs as it has shown promising biological properties.

Current State of Research:

The current state of research on EBGP is focused on the synthesis of novel benzylidene derivatives of carbohydrates, the development of new synthetic methods, and the evaluation of the biological properties of these compounds.

Potential Implications in Various Fields of Research and Industry:

EBGP has potential implications in various fields of research and industry including organic synthesis, drug discovery, and food technology. EBGP could be used as a starting point for developing potential drugs that can target different types of cancer and antimicrobial infections. EBGP can also be used to develop functional food ingredients that can provide additional health benefits to consumers.

Limitations and Future Directions:

EBGP has limitations in terms of its solubility and stability in water. This could limit its use in applications that require high solubility in water. Future research should focus on improving the solubility and stability of EBGP in water to increase its potential applications. Some of the future directions that can be explored are: 1) synthesis of novel benzylidene derivatives of carbohydrates with improved biological activity and water solubility, 2) development of new synthetic methods for EBGP derivatives that can be used for more efficient production, 3) investigation of the potential application of EBGP in cosmetics, and 4) development of EBGP based sensors for the detection of biomolecules.

In conclusion, EBGP is a compound with unique properties and potential applications in various fields of research and industry. Future research should focus on exploring new synthetic methods and investigating potential applications in different fields.

CAS Number101833-22-1
Product NameEthyl 4,6-O-benzylidene-b-D-galactopyranoside
IUPAC Name(4aR,6R,7R,8R,8aR)-6-ethoxy-2-phenyl-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxine-7,8-diol
Molecular FormulaC15H20O6
Molecular Weight296.32 g/mol
InChIInChI=1S/C15H20O6/c1-2-18-15-12(17)11(16)13-10(20-15)8-19-14(21-13)9-6-4-3-5-7-9/h3-7,10-17H,2,8H2,1H3/t10-,11-,12-,13+,14?,15-/m1/s1
InChI KeyUWCTXXNFSDZRJM-JDBBLOKJSA-N
SMILESCCOC1C(C(C2C(O1)COC(O2)C3=CC=CC=C3)O)O
Canonical SMILESCCOC1C(C(C2C(O1)COC(O2)C3=CC=CC=C3)O)O
Isomeric SMILESCCO[C@H]1[C@@H]([C@H]([C@@H]2[C@H](O1)COC(O2)C3=CC=CC=C3)O)O
CAS No: 101833-22-1 MDL No: MFCD07367505 Chemical Formula: C15H20O6 Molecular Weight: 296.32


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