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  • 3006-48-2, D-五苯甲酰基半乳糖, CAS:3006-48-2
3006-48-2, D-五苯甲酰基半乳糖, CAS:3006-48-2

3006-48-2, D-五苯甲酰基半乳糖, CAS:3006-48-2

3006-48-2 ,Penta-O-benzoyl-D-galactopyranoside,
D-五苯甲酰基半乳糖,
CAS:3006-48-2
C41H32O11 / 700.69
MFCD09841153

1,2,3,4,6-Penta-O-benzoyl-D-galactopyranoside

D-五苯甲酰基半乳糖,

1,2,3,4,6-Penta-O-benzoyl-D-galactopyranoside, commonly known as PBG, is a derivative of D-galactose. It is a white crystalline powder that is soluble in methanol and insoluble in water. PBG has been extensively studied for its potential applications in various fields of research and industry, including as a chiral building block, carbohydrate chemistry, and as a starting material for the synthesis of numerous bioactive molecules.

Synthesis and Characterization:

PBG can be synthesized by acylating D-galactose with benzoyl chloride. The process of synthesis involves several steps, including derivatization, protection, and deprotection. PBG can be characterized by various methods, including Nuclear Magnetic Resonance (NMR), Fourier Transform Infrared Spectroscopy (FT-IR), and Mass Spectrometry (MS).

Analytical Methods:

PBG can be analyzed by various analytical methods, including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), and Thin Layer Chromatography (TLC). These methods are used to determine the purity, identity, and concentration of PBG.

Biological Properties:

Recent studies have shown that PBG possesses several biological properties, such as antioxidant, antimicrobial, and antitumor activities. PBG has been found to have inhibitory effects on the growth of various cancer cells, including breast cancer, lung cancer, and pancreatic cancer cells.

Toxicity and Safety in Scientific Experiments:

Studies on the safety and toxicity of PBG are limited, and more research is needed to fully understand its effects on human health. However, the available literature suggests that PBG is relatively safe and non-toxic to human cells.

Applications in Scientific Experiments:

PBG has been widely used as a chiral building block in the synthesis of various bioactive molecules. It has also been used as a starting material for the synthesis of various glycosylation reagents and carbohydrate-based nanoparticles.

Current State of Research:

Research on PBG has been ongoing for several decades, and its potential applications in various fields of research and industry continue to be explored. Recent studies have focused on its biological activities, pharmaceutical applications, and its use as a chiral building block.

Potential Implications in Various Fields of Research and Industry:

PBG has potential applications in various fields of research and industry, including pharmaceuticals, cosmetics, and food products. Its ability to act as a chiral building block and its antioxidant and antimicrobial properties make it an attractive compound for various applications.

Limitations and Future Directions:

Despite its potential applications, PBG has certain limitations, such as its limited solubility in water, which may limit its use in certain applications. Further research is needed to fully understand its biological effects and potential toxicity. Future directions for research on PBG include exploring its potential as a therapeutic agent for cancer treatment and as an antimicrobial agent in food products.

In conclusion, PBG is an important compound that has a wide range of potential applications in various fields of research and industry. Its unique properties and ability to act as a chiral building block make it an attractive compound for numerous applications. However, further research is needed to fully understand its effects on human health and to explore its potential applications in new fields.

CAS Number3006-48-2
Product Name1,2,3,4,6-Penta-O-benzoyl-D-galactopyranoside
IUPAC Name[(3S,6S)-3,4,5,6-tetrabenzoyloxyoxan-2-yl]methyl benzoate
Molecular FormulaC₄₁H₃₂O₁₁
Molecular Weight700.69
InChIInChI=1S/C41H32O11/c42-36(27-16-6-1-7-17-27)47-26-32-33(49-37(43)28-18-8-2-9-19-28)34(50-38(44)29-20-10-3-11-21-29)35(51-39(45)30-22-12-4-13-23-30)41(48-32)52-40(46)31-24-14-5-15-25-31/h1-25,32-35,41H,26H2/t32?,33-,34?,35?,41-/m0/s1
SMILESC1=CC=C(C=C1)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC=CC=C3)OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6
SynonymsD-Galactopyranose 1,2,3,4,6-Pentabenzoate; D-Galactose, 1,2,3,4,6-Pentabenzoate;

CAS No: 3006-48-2 Synonyms: D-Galactopyranose 1,2,3,4,6-pentabenzoateD-Galactose, 1,2,3,4,6-pentabenzoate  MDL No: MFCD09841153 Chemical Formula: C41H32O11 Molecular Weight: 700.69

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