Cas no 1261948-50-8 (4-(3-Chloro-2-methylphenyl)-2-methoxyphenol)
4-(3-Chloro-2-methylphenyl)-2-methoxyphenol Chemical and Physical Properties
Names and Identifiers
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- DTXSID00685593
- 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol, 95%
- MFCD18315158
- 1261948-50-8
- 3'-Chloro-3-methoxy-2'-methyl[1,1'-biphenyl]-4-ol
- 4-(3-CHLORO-2-METHYLPHENYL)-2-METHOXYPHENOL
- 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol
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- MDL: MFCD18315158
- Inchi: 1S/C14H13ClO2/c1-9-11(4-3-5-12(9)15)10-6-7-13(16)14(8-10)17-2/h3-8,16H,1-2H3
- InChI Key: BUJMAPILBCLBSR-UHFFFAOYSA-N
- SMILES: ClC1=CC=CC(=C1C)C1C=CC(=C(C=1)OC)O
Computed Properties
- Exact Mass: 248.0604073Da
- Monoisotopic Mass: 248.0604073Da
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 17
- Rotatable Bond Count: 2
- Complexity: 246
- 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: 4.2
- Topological Polar Surface Area: 29.5?2
4-(3-Chloro-2-methylphenyl)-2-methoxyphenol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB321337-5 g |
4-(3-Chloro-2-methylphenyl)-2-methoxyphenol, 95%; . |
1261948-50-8 | 95% | 5g |
€1159.00 | 2023-04-26 | |
| abcr | AB321337-5g |
4-(3-Chloro-2-methylphenyl)-2-methoxyphenol, 95%; . |
1261948-50-8 | 95% | 5g |
€1159.00 | 2025-04-21 |
4-(3-Chloro-2-methylphenyl)-2-methoxyphenol Related Literature
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Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
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Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
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Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
Additional information on 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol
Comprehensive Overview of 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol (CAS No. 1261948-50-8)
4-(3-Chloro-2-methylphenyl)-2-methoxyphenol, with the CAS number 1261948-50-8, is a versatile organic compound that has garnered significant attention in the fields of chemistry, biology, and pharmaceutical research. This compound is characterized by its unique structural features, which include a chlorinated and methylated phenyl group attached to a methoxyphenol moiety. These structural elements contribute to its diverse chemical properties and potential applications in various scientific and industrial contexts.
The molecular formula of 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol is C13H13ClO2, and its molecular weight is approximately 236.70 g/mol. The compound's physical properties, such as its melting point, boiling point, and solubility in different solvents, have been extensively studied. These properties are crucial for understanding its behavior in various chemical reactions and its suitability for specific applications.
In recent years, 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol has been the subject of numerous research studies due to its potential biological activities. One of the key areas of interest is its anti-inflammatory properties. Studies have shown that this compound can effectively inhibit the production of pro-inflammatory cytokines, such as interleukin-6 (IL-6) and tumor necrosis factor-alpha (TNF-α), making it a promising candidate for the development of anti-inflammatory drugs.
Beyond its anti-inflammatory effects, 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol has also demonstrated antioxidant properties. Antioxidants play a crucial role in neutralizing free radicals and preventing oxidative stress, which is implicated in various diseases, including cardiovascular disorders and neurodegenerative conditions. Research has indicated that this compound can scavenge free radicals and protect cells from oxidative damage, further expanding its potential therapeutic applications.
In the realm of pharmaceutical research, 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol has been explored for its potential as a lead compound in drug discovery. Its unique structure and biological activities make it an attractive starting point for the development of new drugs targeting specific diseases. For instance, studies have investigated its ability to modulate specific enzymes and receptors involved in disease pathways, such as cyclooxygenase (COX) enzymes and nuclear factor-kappa B (NF-κB) signaling pathways.
The synthesis of 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol has been optimized using various methods to improve yield and purity. Common synthetic routes involve the reaction of 3-chloro-2-methylbenzene with 2-methoxyphenol under controlled conditions. These methods have been refined to ensure high efficiency and scalability, making it feasible for large-scale production in industrial settings.
Safety and toxicity profiles are critical considerations for any compound with potential pharmaceutical applications. Extensive toxicological studies have been conducted on 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol to assess its safety profile. These studies have generally shown that the compound is well-tolerated at therapeutic doses, with minimal adverse effects observed in preclinical models. However, ongoing research is necessary to fully understand its long-term safety and potential side effects in human subjects.
In conclusion, 4-(3-Chloro-2-methylphenyl)-2-methoxyphenol (CAS No. 1261948-50-8) is a multifaceted compound with significant potential in various scientific and industrial applications. Its unique chemical structure, coupled with its anti-inflammatory and antioxidant properties, makes it a valuable candidate for further research and development in the fields of chemistry, biology, and pharmaceuticals. As research continues to advance, it is likely that new applications and therapeutic uses for this compound will be discovered, further highlighting its importance in modern scientific endeavors.
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