Cas no 86817-77-8 (2-4-(propan-2-yloxy)phenylethan-1-ol)
2-4-(propan-2-yloxy)phenylethan-1-ol Chemical and Physical Properties
Names and Identifiers
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- 2-(4-propan-2-yloxyphenyl)ethanol
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- 2-4-(propan-2-yloxy)phenylethan-1-ol
- AKOS000279832
- IVMMFYBOPVQEIK-UHFFFAOYSA-N
- CS-0355223
- 2-[4-(propan-2-yloxy)phenyl]ethan-1-ol
- 2-(4-isopropoxyphenyl)ethanol
- NSC20709
- DTXSID60281196
- 86817-77-8
- SCHEMBL833204
- NSC-20709
- EN300-1634237
- 2-(4-Isopropoxyphenyl)ethan-1-ol
- DS-003377
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- MDL: MFCD08694208
- Inchi: 1S/C11H16O2/c1-9(2)13-11-5-3-10(4-6-11)7-8-12/h3-6,9,12H,7-8H2,1-2H3
- InChI Key: IVMMFYBOPVQEIK-UHFFFAOYSA-N
- SMILES: O(C1C=CC(=CC=1)CCO)C(C)C
Computed Properties
- Exact Mass: 180.115029749g/mol
- Monoisotopic Mass: 180.115029749g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 13
- Rotatable Bond Count: 4
- Complexity: 126
- 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: 1.6
- Topological Polar Surface Area: 29.5?2
2-4-(propan-2-yloxy)phenylethan-1-ol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1634237-1g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 1g |
$414.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-5g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 5g |
$1199.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-10g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 10g |
$1778.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-0.05g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 0.05g |
$348.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-0.1g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 0.1g |
$364.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-0.25g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 0.25g |
$381.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-0.5g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 0.5g |
$397.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-1.0g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 1g |
$914.0 | 2023-06-04 | ||
| Enamine | EN300-1634237-2.5g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 2.5g |
$810.0 | 2023-08-31 | ||
| Enamine | EN300-1634237-5.0g |
2-[4-(propan-2-yloxy)phenyl]ethan-1-ol |
86817-77-8 | 5g |
$2650.0 | 2023-06-04 |
2-4-(propan-2-yloxy)phenylethan-1-ol Related Literature
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J. Xu,T. J. Carrocci,A. A. Hoskins Chem. Commun., 2016,52, 549-552
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Ziyang Deng,Changwei Chen,Sunliang Cui RSC Adv., 2016,6, 93753-93755
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Gloria Belén Ramírez-Rodríguez,José Manuel Delgado-López,Jaime Gómez-Morales CrystEngComm, 2013,15, 2206-2212
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Hanie Hashtroudi,Ian D. R. Mackinnon J. Mater. Chem. C, 2020,8, 13108-13126
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
Additional information on 2-4-(propan-2-yloxy)phenylethan-1-ol
Comprehensive Overview of 2-4-(propan-2-yloxy)phenylethan-1-ol (CAS No. 86817-77-8): Properties, Applications, and Industry Insights
In the realm of specialty chemicals, 2-4-(propan-2-yloxy)phenylethan-1-ol (CAS No. 86817-77-8) stands out as a versatile compound with growing relevance across multiple industries. This aromatic alcohol derivative, characterized by its unique propan-2-yloxy and phenylethan-1-ol functional groups, has garnered attention for its potential in fragrance formulations, pharmaceutical intermediates, and organic synthesis. As sustainability and green chemistry dominate modern research trends, this compound's role in eco-friendly solvent systems and bio-based material production aligns perfectly with current market demands.
The molecular structure of 2-4-(propan-2-yloxy)phenylethan-1-ol features a phenylethanol backbone modified with an isopropoxy group at the para position, contributing to its balanced hydrophilicity and lipophilicity. This property makes it particularly valuable in cosmetic emulsions, where formulators increasingly seek alternatives to traditional synthetic stabilizers. Recent studies highlight its compatibility with plant-derived surfactants, addressing the clean beauty movement's call for transparent ingredient lists and reduced synthetic additives.
From a synthetic chemistry perspective, CAS 86817-77-8 serves as a crucial building block for flavor and fragrance compounds. Its aromatic alcohol nature allows for straightforward derivatization into esters and ethers, enabling creation of novel scent profiles that respond to consumer preferences for long-lasting perfumes and natural-identical fragrances. The compound's stability under various pH conditions makes it particularly attractive for personal care products requiring extended shelf life.
Industrial applications of 2-4-(propan-2-yloxy)phenylethan-1-ol extend to polymer modification, where it functions as a plasticizer alternative in certain biodegradable resins. With the global push toward circular economy models, researchers are investigating its potential as a renewable content enhancer in bio-based plastics. The compound's ability to improve material flexibility without compromising thermal stability positions it as an interesting candidate for sustainable packaging solutions.
Analytical characterization of 86817-77-8 reveals excellent chromatographic properties, making it useful as a reference standard in HPLC methods for quality control of related compounds. Laboratories focusing on natural product analysis frequently employ derivatives of this chemical as internal standards when quantifying plant-derived phenolics. The growing demand for authenticity testing in botanical extracts and essential oils has further increased its importance in analytical chemistry workflows.
Safety profiles and regulatory status of 2-4-(propan-2-yloxy)phenylethan-1-ol remain favorable for most commercial applications. Unlike some conventional aromatic alcohols, this compound demonstrates improved biodegradation characteristics in environmental studies, answering industry needs for greener chemical alternatives. Formulators appreciate its compliance with major cosmetic regulations including EU and ASEAN standards, facilitating global product development.
Emerging research explores the compound's potential in advanced material science, particularly in liquid crystal formulations and organic electronics. Its molecular geometry and electron-donating properties show promise for modifying charge transport layers in OLED devices. As the electronics industry seeks more sustainable components, derivatives of CAS 86817-77-8 may contribute to next-generation bio-compatible displays and flexible electronics.
The synthesis and production of 2-4-(propan-2-yloxy)phenylethan-1-ol continue to evolve with green chemistry principles. Recent patents describe catalytic methods that significantly improve atom economy while reducing energy consumption during manufacturing. These advancements support the chemical industry's transition toward carbon-neutral production and help manufacturers meet increasingly stringent sustainability benchmarks for specialty chemicals.
Market analysts project steady growth for 86817-77-8 and related compounds, driven by expanding applications in high-performance coatings and adhesive formulations. Its ability to enhance substrate wetting and film formation makes it valuable in water-based systems that dominate today's low-VOC product segments. As regulations on volatile organic compounds tighten globally, formulators increasingly turn to such modified aromatic alcohols as functional additives.
In conclusion, 2-4-(propan-2-yloxy)phenylethan-1-ol (CAS No. 86817-77-8) represents a compelling example of how molecular innovation can address multiple contemporary challenges. From enabling sustainable product development to supporting cutting-edge material science, this compound's versatility ensures its continued relevance across diverse industries. As research uncovers new applications and improved synthetic routes, its role in green chemistry initiatives and bio-based economies will likely expand further in coming years.
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