Cas no 1261933-93-0 ([1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy)-)
[1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy)- Chemical and Physical Properties
Names and Identifiers
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- [1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy)-
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- MDL: MFCD18316400
- Inchi: 1S/C13H7Cl2F3O2/c14-8-1-2-11(12(15)5-8)7-3-9(19)6-10(4-7)20-13(16,17)18/h1-6,19H
- InChI Key: UPYLJCSENOBRJF-UHFFFAOYSA-N
- SMILES: C1(C2=CC=C(Cl)C=C2Cl)=CC(OC(F)(F)F)=CC(O)=C1
[1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy)- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB322608-5 g |
5-(2,4-Dichlorophenyl)-3-trifluoromethoxyphenol, 95%; . |
1261933-93-0 | 95% | 5g |
€1159.00 | 2023-06-21 | |
| abcr | AB322608-5g |
5-(2,4-Dichlorophenyl)-3-trifluoromethoxyphenol, 95%; . |
1261933-93-0 | 95% | 5g |
€1159.00 | 2025-02-21 |
[1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy)- Related Literature
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Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
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Piotr Szcze?niak,Sebastian Stecko RSC Adv., 2015,5, 30882-30888
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Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
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Priyambada Nayak,Tanmaya Badapanda,Anil Kumar Singh,Simanchalo Panigrahi RSC Adv., 2017,7, 16319-16331
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M. Sheykhan,S. Khani,S. Shaabanzadeh,M. Joafshan Green Chem., 2017,19, 5940-5948
Additional information on [1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy)-
Chemical Profile of [1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy) (CAS No. 1261933-93-0)
[1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy) is a sophisticated organic compound that has garnered significant attention in the field of pharmaceutical and agrochemical research due to its unique structural and functional properties. This compound, identified by the CAS number 1261933-93-0, belongs to the class of biphenyl derivatives, which are widely studied for their potential applications in various chemical syntheses and biological assays.
The molecular structure of this compound features a biphenyl core substituted with chloro and trifluoromethoxy groups at specific positions. The presence of these functional groups imparts distinct reactivity and interaction capabilities, making it a valuable intermediate in the synthesis of more complex molecules. Specifically, the [1,1'-Biphenyl]-3-ol moiety serves as a versatile scaffold for further chemical modifications, while the 2',4'-dichloro and 5-(trifluoromethoxy) substituents enhance its utility in various synthetic pathways.
In recent years, there has been a growing interest in biphenyl derivatives due to their role as key intermediates in the development of novel pharmaceuticals and agrochemicals. The compound [1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy) has been extensively studied for its potential applications in medicinal chemistry. Researchers have explored its use as a precursor in the synthesis of bioactive molecules that exhibit inhibitory effects on various biological targets. For instance, studies have shown that derivatives of this compound can interact with enzymes and receptors involved in metabolic pathways, making them promising candidates for therapeutic intervention.
One of the most compelling aspects of this compound is its structural flexibility, which allows for diverse chemical modifications. The chloro and trifluoromethoxy groups provide reactive sites for further functionalization, enabling the synthesis of a wide range of analogues with tailored properties. This versatility has made [1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy) a valuable tool in drug discovery programs aimed at identifying new therapeutic agents.
Moreover, the compound's stability under various reaction conditions makes it an attractive choice for industrial applications. Its ability to withstand harsh chemical environments while maintaining structural integrity ensures that it can be effectively utilized in large-scale synthetic processes. This stability is particularly important in pharmaceutical manufacturing, where consistency and reliability are paramount.
Recent advancements in computational chemistry have further enhanced the understanding of [1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy). Molecular modeling studies have provided insights into its interactions with biological targets, helping researchers predict its potential efficacy and side effects. These computational approaches have complemented experimental investigations, leading to a more comprehensive understanding of its pharmacological properties.
The agrochemical sector has also benefited from the study of this compound. Its derivatives have been investigated for their potential as pesticides and herbicides due to their ability to disrupt essential biological processes in pests and weeds. The chloro and trifluoromethoxy groups contribute to its bioactivity by enhancing binding affinity to target enzymes and receptors. This has opened up new avenues for developing environmentally friendly agrochemicals that are effective yet less harmful to non-target organisms.
In conclusion, [1,1'-Biphenyl]-3-ol, 2',4'-dichloro-5-(trifluoromethoxy) (CAS No. 1261933-93-0) is a multifaceted compound with significant potential in pharmaceutical and agrochemical applications. Its unique structural features and reactivity make it an invaluable intermediate in synthetic chemistry. As research continues to uncover new applications for this compound, it is likely to play an increasingly important role in the development of innovative drugs and crop protection agents.
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