Cas no 124728-90-1 (2,3-DIFLUOROHYDROQUINONE)
2,3-DIFLUOROHYDROQUINONE Chemical and Physical Properties
Names and Identifiers
-
- 2,3-DIFLUOROHYDROQUINONE
- 1,4-Benzenediol,2,3-difluoro-(9CI)
- 2,3-difluorobenzene-1,4-diol
- 1,4-Benzenediol,2,3-difluoro
- 2,3-Difluoro-4-hydroxyphenol
- 2,3-DIFLUORO-HYDROQUINONE
- 2,3-DI-FURAN-2-YL-QUINOXALINE-6-CARBOXYLIC ACID
- E89720
- A805284
- AKOS006344274
- MFCD04038791
- CS-0192217
- DTXSID00452449
- 1,4-Benzenediol,2,3-difluoro-
- 1,4-BENZENEDIOL, 2,3-DIFLUORO-
- SCHEMBL1512796
- QLKWZXXUWUOXCH-UHFFFAOYSA-N
- 2,3-DIFLUORO-1,4-BENZENEDIOL
- 2,3-bis(fluoranyl)benzene-1,4-diol
- 124728-90-1
-
- MDL: MFCD04038791
- Inchi: 1S/C6H4F2O2/c7-5-3(9)1-2-4(10)6(5)8/h1-2,9-10H
- InChI Key: QLKWZXXUWUOXCH-UHFFFAOYSA-N
- SMILES: FC1C(=C(C=CC=1O)O)F
Computed Properties
- Exact Mass: 146.01800
- Monoisotopic Mass: 146.01793569g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 10
- Rotatable Bond Count: 0
- Complexity: 106
- 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: 1.4
- Topological Polar Surface Area: 40.5?2
Experimental Properties
- Color/Form: 粉紅色晶體
- Density: 1.542±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 124-126 oC
- Boiling Point: 247.9±35.0 oC (760 Torr),
- Flash Point: 103.7±25.9 oC,
- Refractive Index: 1.546
- Solubility: Slightly soluble (1.9 g/l) (25 o C),
- PSA: 40.46000
- LogP: 1.37600
2,3-DIFLUOROHYDROQUINONE Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB151131-1 g |
2,3-Difluoro-hydroquinone; 97% |
124728-90-1 | 1 g |
€248.00 | 2023-07-20 | ||
| abcr | AB151131-5 g |
2,3-Difluoro-hydroquinone; 97% |
124728-90-1 | 5 g |
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| Apollo Scientific | PC408062-250mg |
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124728-90-1 | 97% | 250mg |
£36.00 | 2023-09-02 | |
| Apollo Scientific | PC408062-1g |
2,3-Difluorohydroquinone |
124728-90-1 | 97% | 1g |
£101.00 | 2023-09-02 | |
| Apollo Scientific | PC408062-5g |
2,3-Difluorohydroquinone |
124728-90-1 | 97% | 5g |
£364.00 | 2022-03-29 | |
| abcr | AB151131-1g |
2,3-Difluoro-hydroquinone, 97%; . |
124728-90-1 | 97% | 1g |
€248.00 | 2025-04-21 | |
| abcr | AB151131-5g |
2,3-Difluoro-hydroquinone, 97%; . |
124728-90-1 | 97% | 5g |
€444.00 | 2025-04-21 | |
| Aaron | AR000ND9-1g |
1,4-Benzenediol, 2,3-difluoro- |
124728-90-1 | 97% | 1g |
$587.00 | 2025-02-12 | |
| 1PlusChem | 1P000N4X-250mg |
1,4-Benzenediol, 2,3-difluoro- |
124728-90-1 | 250mg |
$88.00 | 2024-07-10 | ||
| 1PlusChem | 1P000N4X-1g |
1,4-Benzenediol, 2,3-difluoro- |
124728-90-1 | 1g |
$180.00 | 2024-07-10 |
2,3-DIFLUOROHYDROQUINONE Suppliers
2,3-DIFLUOROHYDROQUINONE Related Literature
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Suji Lee,Min Su Han Chem. Commun., 2021,57, 9450-9453
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Bidou Wang,Xifeng Chen Analyst, 2014,139, 5695-5699
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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Xue-Ying Wang,Ying Pei,Min Xie,Zi-He Jin,Ya-Shi Xiao,Yang Wang,Li-Na Zhang,Yan Li,Wei-Hua Huang Lab Chip, 2015,15, 1178-1187
Additional information on 2,3-DIFLUOROHYDROQUINONE
2,3-DIFLUOROHYDROQUINONE: A Comprehensive Overview
2,3-DIFLUOROHYDROQUINONE, also known by its CAS number 124728-90-1, is a chemical compound that has garnered significant attention in the scientific community due to its unique properties and potential applications. This compound belongs to the class of hydroquinones, which are known for their role in various biological and chemical processes. The presence of two fluorine atoms at the 2 and 3 positions of the hydroquinone ring introduces distinct electronic and structural characteristics, making it a subject of interest in both academic research and industrial applications.
The synthesis of 2,3-DIFLUOROHYDROQUINONE involves a series of carefully controlled reactions. Recent studies have focused on optimizing the synthesis process to enhance yield and purity. For instance, researchers have explored the use of fluorinating agents under specific conditions to achieve the desired substitution pattern. These advancements not only improve the efficiency of production but also pave the way for larger-scale manufacturing, which is crucial for its commercialization.
2,3-DIFLUOROHYDROQUINONE exhibits unique chemical reactivity due to the electron-withdrawing nature of the fluorine atoms. This property makes it a valuable compound in various chemical transformations. For example, it has been utilized as a precursor in the synthesis of complex organic molecules, including pharmaceutical intermediates. The compound's ability to undergo nucleophilic aromatic substitution reactions under mild conditions has been particularly noteworthy, as it allows for the construction of diverse molecular architectures.
In terms of applications, 2,3-DIFLUOROHYDROQUINONE has shown promise in several fields. One area of growing interest is its potential use in materials science. Researchers have investigated its role in the development of advanced polymers and coatings. The compound's ability to form stable cross-links under certain conditions makes it a candidate for high-performance materials with enhanced mechanical and thermal properties.
The pharmacological properties of 2,3-DIFLUOROHYDROQUINONE have also been a focal point of recent studies. Preclinical research suggests that it may possess antioxidant and anti-inflammatory activities, which could be harnessed for therapeutic purposes. Additionally, its ability to modulate cellular signaling pathways has led to exploratory studies in oncology, where it may serve as a lead compound for anticancer drug development.
The environmental impact and toxicity profile of 2,3-DIFLUOROHYDROQUINONE are critical considerations for its safe handling and application. Recent toxicological studies have evaluated its effects on aquatic organisms and soil microbiota. These studies aim to provide insights into its potential ecological risks and guide regulatory decisions regarding its use.
In conclusion, 2,3-DIFLUOROHYDROQUINONE, with its CAS number 124728-90-1, represents a versatile compound with a wide range of applications across multiple disciplines. Ongoing research continues to uncover new aspects of its chemistry and utility, underscoring its importance in both academic and industrial settings.
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