Cas no 1214367-67-5 (2-(3',2-Difluorobiphenyl-3-yl)acetic acid)
2-(3',2-Difluorobiphenyl-3-yl)acetic acid Chemical and Physical Properties
Names and Identifiers
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- 2-(3',2-Difluorobiphenyl-3-yl)acetic acid
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- Inchi: 1S/C14H10F2O2/c15-11-5-1-3-9(7-11)12-6-2-4-10(14(12)16)8-13(17)18/h1-7H,8H2,(H,17,18)
- InChI Key: WUNGUTVAAICTRY-UHFFFAOYSA-N
- SMILES: FC1=C(C=CC=C1C1C=CC=C(C=1)F)CC(=O)O
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 4
- Heavy Atom Count: 18
- Rotatable Bond Count: 3
- Complexity: 296
- XLogP3: 3.2
- Topological Polar Surface Area: 37.3
2-(3',2-Difluorobiphenyl-3-yl)acetic acid Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A011001867-250mg |
2-(3',2-Difluorobiphenyl-3-yl)acetic acid |
1214367-67-5 | 97% | 250mg |
$494.40 | 2023-09-04 | |
| Alichem | A011001867-500mg |
2-(3',2-Difluorobiphenyl-3-yl)acetic acid |
1214367-67-5 | 97% | 500mg |
$847.60 | 2023-09-04 | |
| Alichem | A011001867-1g |
2-(3',2-Difluorobiphenyl-3-yl)acetic acid |
1214367-67-5 | 97% | 1g |
$1519.80 | 2023-09-04 |
2-(3',2-Difluorobiphenyl-3-yl)acetic acid Related Literature
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
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Hamid Heydari,Mohammad B. Gholivand New J. Chem., 2017,41, 237-244
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3. An integrated microfluidic 3D tumor system for parallel and high-throughput chemotherapy evaluation?Dan Liu,Rui Hu,Zhongchao Huang,Meilin Sun,Kai Han Analyst, 2020,145, 6447-6455
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Huiying Xu,Lu Zheng,Yu Zhou,Bang-Ce Ye Analyst, 2021,146, 5542-5549
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
Additional information on 2-(3',2-Difluorobiphenyl-3-yl)acetic acid
2-(3',2-Difluorobiphenyl-3-yl)acetic Acid: A Comprehensive Overview
The compound with CAS No. 1214367-67-5, known as 2-(3',2-Difluorobiphenyl-3-yl)acetic acid, is a highly specialized organic compound that has garnered significant attention in the fields of pharmaceutical chemistry and materials science. This compound is characterized by its unique structure, which includes a biphenyl ring system substituted with two fluorine atoms and an acetic acid moiety. The presence of fluorine atoms in the molecule introduces interesting electronic and steric properties, making it a valuable compound for various applications.
The synthesis of 2-(3',2-Difluorobiphenyl-3-yl)acetic acid typically involves multi-step organic reactions, often utilizing coupling reactions and fluorination techniques. Recent advancements in catalytic methods have enabled more efficient and selective syntheses, reducing production costs and improving the overall yield. The compound's physical properties, such as its melting point, solubility, and stability under various conditions, have been extensively studied to optimize its use in different industrial applications.
In terms of applications, 2-(3',2-Difluorobiphenyl-3-yl)acetic acid has shown promise in the development of novel pharmaceutical agents. Its ability to modulate specific biological pathways makes it a potential candidate for treating various diseases, including cancer and neurodegenerative disorders. Recent studies have highlighted its role as a ligand in metalloenzyme inhibition, where its fluorinated biphenyl group plays a critical role in binding affinity and selectivity.
Beyond pharmacology, this compound has also found applications in materials science. Its unique electronic properties make it suitable for use in organic electronics, particularly in the development of advanced polymers and semiconductors. Researchers have explored its potential as a building block for creating high-performance organic light-emitting diodes (OLEDs) and photovoltaic materials. The incorporation of fluorine atoms enhances the material's stability under harsh conditions, making it a valuable component in next-generation electronic devices.
The environmental impact of 2-(3',2-Difluorobiphenyl-3-yl)acetic acid has also been a topic of interest. Studies have shown that while the compound exhibits moderate biodegradability, its persistence in certain environmental conditions requires careful management during production and disposal. Regulatory agencies have implemented guidelines to ensure safe handling and minimize ecological risks associated with this compound.
In conclusion, 2-(3',2-Difluorobiphenyl-3-yl)acetic acid is a versatile compound with a wide range of applications across multiple disciplines. Its unique chemical structure, coupled with recent advancements in synthesis and application techniques, positions it as a key player in future scientific innovations. As research continues to uncover new potentials for this compound, its role in advancing technology and medicine is expected to grow significantly.
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