Cas no 13391-32-7 (Phenol, 2-ethyl-4-methoxy-)
Phenol, 2-ethyl-4-methoxy- Chemical and Physical Properties
Names and Identifiers
-
- Phenol, 2-ethyl-4-methoxy-
- 2-ethyl-4-methoxyphenol
- DTXSID00516030
- SCHEMBL805304
- MB23776
- 13391-32-7
-
- Inchi: 1S/C9H12O2/c1-3-7-6-8(11-2)4-5-9(7)10/h4-6,10H,3H2,1-2H3
- InChI Key: RPDJASOWDQGWJF-UHFFFAOYSA-N
- SMILES: O(C)C1=CC=C(C(=C1)CC)O
Computed Properties
- Exact Mass: 152.083729621g/mol
- Monoisotopic Mass: 152.083729621g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 11
- Rotatable Bond Count: 2
- Complexity: 114
- 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: nothing
- Tautomer Count: 3
- Surface Charge: 0
- Topological Polar Surface Area: 29.5?2
Phenol, 2-ethyl-4-methoxy- Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1956126-1g |
2-Ethyl-4-methoxyphenol |
13391-32-7 | 97% | 1g |
¥7534.00 | 2024-08-09 |
Phenol, 2-ethyl-4-methoxy- Related Literature
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Huading Zhang,Lee R. Moore,Maciej Zborowski,P. Stephen Williams,Shlomo Margel,Jeffrey J. Chalmers Analyst, 2005,130, 514-527
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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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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Partha Laskar,Christine Dufès Nanoscale Adv., 2021,3, 6007-6026
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Vishwesh Venkatraman,Marco Foscato,Vidar R. Jensen,Bj?rn K?re Alsberg J. Mater. Chem. A, 2015,3, 9851-9860
Additional information on Phenol, 2-ethyl-4-methoxy-
Introduction to 2-Ethyl-4-Methoxyphenol (CAS No. 13391-32-7)
2-Ethyl-4-methoxyphenol, also known by its CAS number 13391-32-7, is a versatile organic compound with a wide range of applications in the chemical and pharmaceutical industries. This compound is characterized by its unique molecular structure, which includes an ethyl group and a methoxy group attached to a phenolic ring. The combination of these functional groups imparts specific chemical and physical properties that make it valuable in various research and industrial settings.
The molecular formula of 2-Ethyl-4-methoxyphenol is C9H12O2, and its molecular weight is approximately 152.19 g/mol. The compound is a white to off-white crystalline solid at room temperature, with a melting point ranging from 50 to 52°C and a boiling point of around 250°C. It is slightly soluble in water but highly soluble in organic solvents such as ethanol, acetone, and dichloromethane.
In the context of chemical synthesis, 2-Ethyl-4-methoxyphenol serves as an important intermediate for the production of various pharmaceuticals, agrochemicals, and fine chemicals. Its reactivity and stability make it a preferred choice for synthetic routes that require controlled reactions under specific conditions. Recent advancements in synthetic chemistry have further expanded its utility, with researchers exploring novel methods to enhance its yield and purity.
In the pharmaceutical industry, 2-Ethyl-4-methoxyphenol has shown promise in the development of new drugs targeting various diseases. One notable application is in the synthesis of antioxidants, which are crucial for preventing oxidative stress-related conditions such as cardiovascular diseases and neurodegenerative disorders. Studies have demonstrated that derivatives of 2-Ethyl-4-methoxyphenol exhibit potent antioxidant activity, making them potential candidates for therapeutic interventions.
Beyond its pharmaceutical applications, 2-Ethyl-4-methoxyphenol has also found use in the cosmetics industry. Its antimicrobial properties make it suitable for inclusion in formulations designed to prevent microbial contamination. Additionally, its ability to stabilize other active ingredients enhances the overall efficacy and shelf life of cosmetic products.
In the realm of environmental science, research has focused on the biodegradability and environmental impact of 2-Ethyl-4-methoxyphenol. Studies have shown that under certain conditions, this compound can be effectively degraded by microorganisms, reducing its potential for environmental accumulation. This characteristic is particularly important for ensuring the sustainability of industrial processes involving this compound.
The safety profile of 2-Ethyl-4-methoxyphenol has been extensively studied to ensure its safe handling and use. While it is generally considered safe when used under controlled conditions, proper precautions should be taken to avoid inhalation, ingestion, or skin contact. Safety data sheets (SDS) provide detailed information on handling, storage, and disposal procedures to minimize risks associated with its use.
In conclusion, 2-Ethyl-4-methoxyphenol (CAS No. 13391-32-7) is a multifaceted compound with significant potential in various fields. Its unique chemical properties make it an essential component in synthetic routes for pharmaceuticals, agrochemicals, and fine chemicals. Ongoing research continues to uncover new applications and optimize existing processes involving this compound, further solidifying its importance in the scientific community.
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