Cas no 65214-59-7 (2,4-Dichloro-4'-Fluorobenzophenone)
2,4-Dichloro-4'-Fluorobenzophenone Chemical and Physical Properties
Names and Identifiers
-
- (2,4-dichlorophenyl)(4-fluorophenyl)methanone
- methanone, (2,4-dichlorophenyl)(4-fluorophenyl)-
- 2,4-DICHLORO-4'-FLUOROBENZOPHENONE
- 65214-59-7
- SCHEMBL611648
- UVAKGOJIHCGXID-UHFFFAOYSA-N
- EN300-269545
- (2,4-dichlorophenyl)(4-fluorophenyl) methanone
- DTXSID40983823
- Z385412734
- (2,4-dichlorophenyl)-(4-fluorophenyl)methanone
- AKOS006036410
- DS-007714
- CS-0243884
- NSC141024
- MFCD00135179
- NSC-141024
- 2,4-Dichloro-4'-Fluorobenzophenone
-
- MDL: MFCD00135179
- Inchi: 1S/C13H7Cl2FO/c14-9-3-6-11(12(15)7-9)13(17)8-1-4-10(16)5-2-8/h1-7H
- InChI Key: UVAKGOJIHCGXID-UHFFFAOYSA-N
- SMILES: ClC1C=C(C=CC=1C(C1C=CC(=CC=1)F)=O)Cl
Computed Properties
- Exact Mass: 267.98591
- Monoisotopic Mass: 267.9857984g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 17
- Rotatable Bond Count: 2
- Complexity: 277
- 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: 4.5
- Topological Polar Surface Area: 17.1?2
Experimental Properties
- PSA: 17.07
2,4-Dichloro-4'-Fluorobenzophenone Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | D650648-10mg |
2,4-Dichloro-4'-Fluorobenzophenone |
65214-59-7 | 10mg |
$ 50.00 | 2022-06-05 | ||
| TRC | D650648-50mg |
2,4-Dichloro-4'-Fluorobenzophenone |
65214-59-7 | 50mg |
$ 70.00 | 2022-06-05 | ||
| TRC | D650648-100mg |
2,4-Dichloro-4'-Fluorobenzophenone |
65214-59-7 | 100mg |
$ 115.00 | 2022-06-05 | ||
| Enamine | EN300-269545-0.05g |
(2,4-dichlorophenyl)(4-fluorophenyl)methanone |
65214-59-7 | 95.0% | 0.05g |
$39.0 | 2025-02-20 | |
| Enamine | EN300-269545-1g |
(2,4-dichlorophenyl)(4-fluorophenyl)methanone |
65214-59-7 | 95% | 1g |
$241.0 | 2023-09-11 | |
| Enamine | EN300-269545-5g |
(2,4-dichlorophenyl)(4-fluorophenyl)methanone |
65214-59-7 | 95% | 5g |
$701.0 | 2023-09-11 | |
| Enamine | EN300-269545-10g |
(2,4-dichlorophenyl)(4-fluorophenyl)methanone |
65214-59-7 | 95% | 10g |
$1040.0 | 2023-09-11 | |
| Enamine | EN300-269545-0.1g |
(2,4-dichlorophenyl)(4-fluorophenyl)methanone |
65214-59-7 | 95.0% | 0.1g |
$62.0 | 2025-02-20 | |
| Enamine | EN300-269545-0.25g |
(2,4-dichlorophenyl)(4-fluorophenyl)methanone |
65214-59-7 | 95.0% | 0.25g |
$88.0 | 2025-02-20 | |
| Enamine | EN300-269545-0.5g |
(2,4-dichlorophenyl)(4-fluorophenyl)methanone |
65214-59-7 | 95.0% | 0.5g |
$164.0 | 2025-02-20 |
2,4-Dichloro-4'-Fluorobenzophenone Suppliers
2,4-Dichloro-4'-Fluorobenzophenone Related Literature
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Guiying Zhang,Maosheng Cheng,Yanni Li,Keliang Liu,Lifeng Cai Chem. Commun., 2013,49, 11086-11088
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Liao Xiaoqing,Li Ruiyi,Li Zaijun,Sun Xiulan,Wang Zhouping,Liu Junkang New J. Chem., 2015,39, 5240-5248
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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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Joseph H. Bisesi,Tara Sabo-Attwood Environ. Sci.: Nano, 2014,1, 574-583
Additional information on 2,4-Dichloro-4'-Fluorobenzophenone
Comprehensive Analysis of 2,4-Dichloro-4'-Fluorobenzophenone (CAS No. 65214-59-7): Properties, Applications, and Industry Trends
2,4-Dichloro-4'-Fluorobenzophenone (CAS No. 65214-59-7) is a specialized organic compound widely recognized for its unique chemical structure and versatile applications in pharmaceuticals, agrochemicals, and material science. With the increasing demand for high-performance intermediates in synthetic chemistry, this compound has garnered significant attention due to its halogen-substituted benzophenone framework, which enhances reactivity and stability in various reactions. Researchers and manufacturers are actively exploring its potential in photoinitiators, liquid crystal materials, and advanced polymer synthesis, aligning with the growing focus on sustainable and efficient chemical processes.
The molecular structure of 2,4-Dichloro-4'-Fluorobenzophenone features a benzophenone core substituted with two chlorine atoms at the 2- and 4-positions and a fluorine atom at the 4'-position. This configuration imparts distinct electronic properties, making it valuable for UV-curable coatings and electronic materials. Recent studies highlight its role in organic light-emitting diodes (OLEDs), where its electron-withdrawing groups improve charge transport efficiency. As industries shift toward green chemistry, the compound's compatibility with catalytic reactions and low-waste synthesis methods has become a key research focus.
In the pharmaceutical sector, 2,4-Dichloro-4'-Fluorobenzophenone serves as a critical intermediate for active pharmaceutical ingredients (APIs). Its derivatives are investigated for their potential in anticancer agents and central nervous system (CNS) drugs, addressing global health challenges. The compound's bioisosteric properties allow for tailored modifications, meeting the demand for precision medicine. Concurrently, agrochemical applications leverage its stability to develop next-generation pesticides with reduced environmental impact, resonating with the sustainable agriculture movement.
From a commercial perspective, the market for halogenated benzophenones is expanding, driven by advancements in high-performance materials and renewable energy technologies. Suppliers emphasize high-purity grades of CAS No. 65214-59-7 to meet stringent industry standards, while regulatory compliance with REACH and FDA guidelines ensures safe handling. Analytical techniques like HPLC and GC-MS are routinely employed to verify quality, reflecting the compound's importance in quality-critical applications.
Emerging trends also highlight the integration of 2,4-Dichloro-4'-Fluorobenzophenone in nanotechnology and smart materials. Its ability to form stable complexes with metals opens avenues for catalysis and sensor development, aligning with the rise of Industry 4.0. As researchers address challenges like scalability and cost-efficiency, collaborations between academia and industry are accelerating innovation. This compound exemplifies how specialty chemicals can bridge gaps between traditional synthesis and cutting-edge technologies, offering solutions for a resource-conscious future.
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