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  • 341972-98-3 , 5-Bromo-4-chloro-3-indolyl palmitate ,X-Pal
341972-98-3 , 5-Bromo-4-chloro-3-indolyl palmitate ,X-Pal

341972-98-3 , 5-Bromo-4-chloro-3-indolyl palmitate ,X-Pal

Cas:341972-98-3 ,
5-Bromo-4-chloro-3-indolyl palmitate ,X-Pal
C24H35BrClNO2 / 484.90
MFCD00798390

5-Bromo-4-chloro-3-indolyl palmitate ,X-Pal

5-Bromo-4-chloro-3-indolyl palmitate is a modification of the indole group that is attached to the fatty acid. The modification is targeted to specific proteins in cells, which can be measured using several different techniques. 5-Bromo-4-chloro-3-indolyl palmitate has been shown to be efficient and efficient in targeting proteins, with high levels of modification observed on some targets. Factors affecting the efficiency of this modification include the type of cell, experimental conditions, and the technique used for detection.

(5-bromo-4-chloro-1H-indol-3-yl) Hexadecanoate, also known as BCIN, is a chemical compound belonging to the family of indole derivatives. It is an ester formed by the reaction of hexadecanoic acid and BCIN. The compound has gained significant attention in recent years due to its potential applications in various fields of research and industry.

Physical and Chemical Properties:

BCIN is a white crystalline powder with a molecular weight of 523.94 g/mol. It is sparingly soluble in common solvents such as methanol and ethanol but has moderate solubility in DMSO and DMF. The compound is stable at room temperature but needs to be protected from light and moisture. The melting point of BCIN ranges from 121-125°C.

Synthesis and Characterization:

The synthesis of BCIN can be achieved through a two-step reaction involving the condensation of 4-chloro-1H-indole-3-carboxylic acid with SOCl2 followed by esterification with hexadecanol using DMAP as a catalyst. The compound can be characterized by various spectroscopic and analytical methods such as NMR, IR, and MS.

Analytical methods:

The analysis of BCIN can be done through various chromatographic techniques such as HPLC and GC. The purity and identity of the compound can be confirmed using NMR and mass spectroscopy.

Biological Properties:

The potential biological properties of BCIN have been investigated in various studies. It has been reported to possess antitumor activity against different cancer cell lines. Additionally, BCIN has also shown significant anti-inflammatory activity in vitro.

Toxicity and Safety in Scientific Experiments:

The toxicity of BCIN has been studied in animal models, and it has been reported to have low toxicity levels. However, a complete toxicity and safety profile of BCIN still needs to be determined.

Applications in Scientific Experiments:

BCIN has shown potential applications in various fields of research, including medicinal chemistry, material science, and nanotechnology. In medicinal chemistry, BCIN has been explored as a potential anticancer agent. In material science and nanotechnology, BCIN has shown promising applications as a building block for the synthesis of novel materials and in the fabrication of nanostructures.

Current State of Research:

The research on BCIN is ongoing, and many studies are being conducted to explore its potential applications in various fields of research and industry. Recent studies have focused on using BCIN as a building block for the synthesis of multifunctional materials and in targeted drug delivery systems.

Potential Implications in Various Fields of Research and Industry:

The potential implications of BCIN in the fields of research and industry cannot be overstated. BCIN has shown potential applications in diverse fields such as drug development, nanotechnology, and bioimaging. The unique chemical structure of BCIN makes it an attractive candidate for the synthesis of novel materials and the development of targeted drug delivery systems.

Limitations and Future Directions:

Despite the extensive research on BCIN in recent years, there are still many limitations and future directions that need to be investigated. The complete mechanism of action of BCIN as an anticancer agent is not yet understood, and the full toxicity and safety profile of BCIN is yet to be determined. Future studies should aim to address these limitations and explore further applications of BCIN in various fields of research and industry.

Future Directions:

1. Investigating the molecular mechanism of action of BCIN as an anticancer agent

2. Developing targeted drug delivery systems using BCIN as the building block

3. Exploring the potential of BCIN in diagnostic imaging

4. Characterizing the safety profile of BCIN in humans

5. Developing nanotechnology-based applications using BCIN

6. Studying the potential of BCIN as a biosensor

7. Evaluating the antimicrobial activity of BCIN

8. Investigating the potential of BCIN as an antiviral agent

9. Exploring the potential of BCIN in the treatment of neurodegenerative diseases

10. Synthesizing novel compounds based on the structure of BCIN for various applications.

CAS Number341972-98-3
Product Name(5-bromo-4-chloro-1H-indol-3-yl) Hexadecanoate
IUPAC Name(5-bromo-4-chloro-1H-indol-3-yl) hexadecanoate
Molecular FormulaC24H35BrClNO2
Molecular Weight484.9 g/mol
InChIInChI=1S/C24H35BrClNO2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-22(28)29-21-18-27-20-17-16-19(25)24(26)23(20)21/h16-18,27H,2-15H2,1H3
InChI KeyFREDWHLFBOAXBQ-UHFFFAOYSA-N
SMILESCCCCCCCCCCCCCCCC(=O)OC1=CNC2=C1C(=C(C=C2)Br)Cl
Canonical SMILESCCCCCCCCCCCCCCCC(=O)OC1=CNC2=C1C(=C(C=C2)Br)Cl


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