Cas no 114446-57-0 ((1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol)
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol Chemical and Physical Properties
Names and Identifiers
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- (R)-2-chloro-1-(2,4-dichlorophenyl)ethanol
- (R)-2-chloro-1-(2,4-dichlorophenyl)ethan-1-ol
- (1R)-2-chloro-1-(2,4-dichlorophenyl)ethanol
- (1R)-2-chloro-1-(2,4-dichlorophenyl)ethan-1-ol
- Benzenemethanol, 2,4-dichloro-alpha-(chloromethyl)-, (alphaR)-
- NE36400
- WT81677
- C3424
- (r)-2,2',4'-trichloro-1-phenylethan-1-ol
- (R)-2-Chloro-(2',4'-dichlorophenyl)-1-ethanol
- (R)-alpha-(Chloromethyl)-2,4-dichlorobenzyl alcohol
- AKOS032950078
- MFCD09863567
- DB-406172
- EN300-87664
- (R)-alpha-(Chloromethyl)-2,4-dichlorobenzylalcohol
- AS-69603
- 114446-57-0
- XHEPANNURIQWRM-QMMMGPOBSA-N
- SCHEMBL7460986
- A11909
- (1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol
-
- MDL: MFCD09863567
- Inchi: 1S/C8H7Cl3O/c9-4-8(12)6-2-1-5(10)3-7(6)11/h1-3,8,12H,4H2/t8-/m0/s1
- InChI Key: XHEPANNURIQWRM-QMMMGPOBSA-N
- SMILES: ClC[C@@H](C1C=CC(=CC=1Cl)Cl)O
Computed Properties
- Exact Mass: 223.956248 g/mol
- Monoisotopic Mass: 223.956248 g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 12
- Rotatable Bond Count: 2
- Complexity: 142
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 1
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.9
- Topological Polar Surface Area: 20.2
- Molecular Weight: 225.5
Experimental Properties
- Density: 1.447±0.06 g/cm3 (20 oC 760 Torr),
- Melting Point: 46-47 oC
- Solubility: Very slightly soluble (0.36 g/l) (25 o C),
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | C364338-10mg |
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 10mg |
$ 70.00 | 2022-04-28 | ||
| TRC | C364338-50mg |
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 50mg |
$ 210.00 | 2022-04-28 | ||
| TRC | C364338-100mg |
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 100mg |
$ 340.00 | 2022-04-28 | ||
| Chemenu | CM219640-100mg |
(R)-2-chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 95% | 100mg |
$88 | 2022-06-14 | |
| Chemenu | CM219640-250mg |
(R)-2-chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 95% | 250mg |
$154 | 2022-06-14 | |
| Chemenu | CM219640-1g |
(R)-2-chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 95% | 1g |
$301 | 2022-06-14 | |
| SU ZHOU XIN JIA YUAN HUA XUE Technology Co., Ltd. | lj0846-1g |
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 98% | 1g |
¥1398.0 | 2024-07-19 | |
| SU ZHOU XIN JIA YUAN HUA XUE Technology Co., Ltd. | lj0846-100mg |
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | 98% | 100mg |
¥500.0 | 2024-07-19 | |
| Key Organics Ltd | AS-69603-0.25g |
(1R)-2-chloro-1-(2,4-dichlorophenyl)ethan-1-ol |
114446-57-0 | >95% | 0.25g |
£303.00 | 2025-02-08 | |
| SHANG HAI MAI KE LIN SHENG HUA Technology Co., Ltd. | R931717-1g |
(R)-2-Chloro-1-(2,4-dichlorophenyl)ethanol |
114446-57-0 | 98%,99%ee | 1g |
¥93.60 | 2022-08-31 |
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol Suppliers
(1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol Related Literature
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Christopher B. Rodell,Christopher B. Highley,Minna H. Chen,Neville N. Dusaj,Chao Wang,Lin Han,Jason A. Burdick Soft Matter, 2016,12, 7839-7847
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Maomao Hou,Fenglin Zhong,Qiu Jin,Enjiang Liu,Jie Feng,Tengyun Wang,Yue Gao RSC Adv., 2017,7, 34392-34400
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
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Xiaotong Feng,Lei Bian,Jie Ma,Lei Zhou,Xiayan Wang,Guangsheng Guo,Qiaosheng Pu Chem. Commun., 2019,55, 3963-3966
Additional information on (1R)-2-Chloro-1-(2,4-dichlorophenyl)ethan-1-ol
(1R)-2-Chloro-1-(2,4-Dichlorophenyl)Ethan-1-Ol: A Comprehensive Overview
(1R)-2-Chloro-1-(2,4-Dichlorophenyl)Ethan-1-Ol, also known by its CAS No. 114446-57-0, is a versatile organic compound with a unique structure that has garnered significant attention in various scientific domains. This compound is characterized by its chiral center at the ethanol position, which imparts it with distinct optical properties and biological activity. The molecule consists of a chlorinated phenyl ring attached to a hydroxyl-bearing carbon, making it a valuable intermediate in organic synthesis and a potential candidate for pharmacological applications.
Recent advancements in synthetic chemistry have highlighted the importance of chiral compounds like (1R)-2-Chloro-1-(2,4-Dichlorophenyl)Ethan-1-Ol in the development of enantioselective reactions. Researchers have demonstrated that this compound can serve as an efficient building block for constructing complex molecular architectures, particularly in the synthesis of bioactive molecules. Its ability to undergo various functional group transformations has made it a cornerstone in modern drug discovery processes.
In the pharmaceutical industry, (1R)-2-Chloro-1-(2,4-Dichlorophenyl)Ethan-1-Ol has shown promise as a precursor for developing agents targeting specific biological pathways. For instance, studies have explored its role in the synthesis of kinase inhibitors and other enzyme-targeting drugs. The compound's unique stereochemistry allows for precise control over the spatial arrangement of substituents, which is critical for achieving desired pharmacokinetic properties.
Moreover, the environmental impact of (1R)-2-Chloro-1-(2,4-Dichlorophenyl)Ethan-1-Ol has been a topic of recent research interest. Scientists have investigated its biodegradation pathways and toxicity profiles to assess its safety for industrial and therapeutic applications. These studies have provided valuable insights into its potential use in green chemistry initiatives and sustainable chemical manufacturing processes.
The synthesis of (1R)-2-Chloro-1-(2,4-Dichlorophenyl)Ethan-1-Ol typically involves multi-step reactions that require precise control over reaction conditions to ensure high yields and enantiomeric purity. Innovations in catalytic asymmetric synthesis have significantly enhanced the efficiency of these processes, making large-scale production more feasible.
In conclusion, (1R)-2-Chloro-1-(2,4-Dichlorophenyl)Ethan-1-Ol (CAS No. 114446-57-0) stands as a testament to the ingenuity of modern organic chemistry. Its diverse applications across pharmaceuticals, agrochemicals, and materials science underscore its importance as a key intermediate in chemical synthesis. As research continues to uncover new facets of its properties and potential uses, this compound is poised to play an even greater role in advancing scientific and technological frontiers.
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