Cas no 150224-16-1 (1,2,3,6,7-Pentachloronaphthalene)
1,2,3,6,7-Pentachloronaphthalene Chemical and Physical Properties
Names and Identifiers
-
- Naphthalene,1,2,3,6,7-pentachloro-
- 1,2,3,6,7-Pentachloronaphthalene
- 1,2,3,6,7-PENTACHLORONAPHTHALENE 10 μG
- ML IN ISO-OCTANE
- Naphthalene, 1,2,3,6,7-pentachloro
- 150224-16-1
- NS00066953
- DTXSID00164499
- 1,2,3,6,7-Pentachloro-naphthalene
- BDBM50159246
- MKCASBPTHPJCDC-UHFFFAOYSA-N
- starbld0001294
- CHEMBL195537
- Naphthalene, 1,2,3,6,7-pentachloro-
-
- Inchi: 1S/C10H3Cl5/c11-6-1-4-2-8(13)10(15)9(14)5(4)3-7(6)12/h1-3H
- InChI Key: MKCASBPTHPJCDC-UHFFFAOYSA-N
- SMILES: ClC1C(=C(C=C2C=C(C(=CC2=1)Cl)Cl)Cl)Cl
Computed Properties
- Exact Mass: 297.86799
- Monoisotopic Mass: 297.868
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 15
- Rotatable Bond Count: 0
- Complexity: 234
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 6.3
- Topological Polar Surface Area: 0?2
Experimental Properties
- Density: 1.638
- Boiling Point: 368.1°Cat760mmHg
- Flash Point: 182.4°C
- Refractive Index: 1.671
- PSA: 0
1,2,3,6,7-Pentachloronaphthalene Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P237985-10mg |
1,2,3,6,7-Pentachloronaphthalene |
150224-16-1 | 10mg |
$207.00 | 2023-05-17 | ||
| TRC | P237985-100mg |
1,2,3,6,7-Pentachloronaphthalene |
150224-16-1 | 100mg |
$ 1800.00 | 2023-09-06 |
1,2,3,6,7-Pentachloronaphthalene Related Literature
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Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
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Gang Pan,Yi-jie Bao,Jie Xu,Tao Liu,Cheng Liu,Yan-yan Qiu,Xiao-jing Shi,Hui Yu,Ting-ting Jia,Xia Yuan,Ze-ting Yuan,Yi-jun Cao RSC Adv., 2016,6, 42109-42119
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3. Estimating and correcting interference fringes in infrared spectra in infrared hyperspectral imagingGhazal Azarfar,Ebrahim Aboualizadeh,Nicholas M. Walter,Simona Ratti,Camilla Olivieri,Alessandra Norici,Michael Nasse,Achim Kohler,Mario Giordano Analyst, 2018,143, 4674-4683
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Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
Additional information on 1,2,3,6,7-Pentachloronaphthalene
Chemical Profile of 1,2,3,6,7-Pentachloronaphthalene (CAS No. 150224-16-1)
1,2,3,6,7-Pentachloronaphthalene, identified by the chemical abstracts service number 150224-16-1, is a chlorinated derivative of naphthalene with a unique structure that has garnered significant attention in the field of chemical and pharmaceutical research. This compound, featuring five chlorine atoms strategically positioned on its benzene-like aromatic ring system, exhibits distinct chemical properties that make it a subject of interest for various applications, particularly in the synthesis of specialized materials and as an intermediate in organic chemistry.
The molecular structure of 1,2,3,6,7-Pentachloronaphthalene contributes to its reactivity and stability under different conditions. The presence of multiple chlorine atoms enhances its electron-withdrawing effect, which can influence its interactions with other molecules. This characteristic is particularly valuable in pharmaceutical research, where such modifications can lead to the development of novel compounds with enhanced biological activity. The compound’s stability under thermal and chemical stress also makes it a candidate for use in industrial processes requiring robust intermediates.
In recent years, 1,2,3,6,7-Pentachloronaphthalene has been studied for its potential applications in the synthesis of liquid crystals and advanced polymers. The chlorine atoms introduce polarity into the molecule, which can be leveraged to improve the material’s properties for specific uses. For instance, researchers have explored its role in creating liquid crystalline materials that exhibit desirable optical and electronic properties. These materials are increasingly important in the development of display technologies and other advanced electronic devices.
Additionally, the compound has found utility in the field of agrochemicals. Its structural features allow it to act as a precursor in the synthesis of certain pesticides and herbicides. The chlorine atoms can be selectively replaced or modified to create derivatives with targeted biological activity against pests or weeds. This approach aligns with the growing demand for environmentally friendly agrochemicals that are effective yet minimize ecological impact.
From a pharmaceutical perspective, 1,2,3,6,7-Pentachloronaphthalene has been investigated as a building block for more complex drug molecules. Its aromatic core can be functionalized to introduce various pharmacophores responsible for biological activity. Researchers have explored its potential in developing antiviral and anticancer agents. The chlorine atoms provide handles for further chemical modifications, enabling the creation of compounds with enhanced binding affinity to biological targets. Such modifications are crucial for improving drug efficacy and reducing side effects.
The synthesis of 1,2,3,6,7-Pentachloronaphthalene typically involves chlorination reactions on naphthalene or its derivatives. Advanced synthetic methodologies have been developed to achieve high selectivity and yield during these processes. Techniques such as catalytic chlorination and photochemical reactions have been employed to optimize the production of this compound. These advancements ensure that researchers can obtain sufficient quantities of 1,2,3,6,7-Pentachloronaphthalene for their studies without compromising purity or efficiency.
The safety profile of 1,2,3,6,7-Pentachloronaphthalene is another critical aspect that has been thoroughly examined. While it is not classified as a hazardous material under standard regulations due to its relatively low reactivity compared to other chlorinated aromatic compounds; proper handling procedures must still be followed to prevent unintended exposure. Studies have focused on understanding its toxicity profile through in vitro and in vivo experiments. These studies aim to establish safe exposure limits and inform potential uses in industrial or laboratory settings.
In conclusion,1 ,2 ,3 ,6 ,7 -Pentachloronaphthalene (CAS No . 150224-16-1) is a versatile compound with applications spanning multiple industries including advanced materials ,agrochemicals ,and pharmaceuticals .Its unique structure offers opportunities for innovation through further chemical modifications .As research continues ,the full potential of this compound is likely to be uncovered ,leading to new applications that benefit society .The ongoing exploration into its properties underscores its importance as a valuable chemical intermediate .
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