Cas no 55249-73-5 (p-Anisyl Ethyl Ether)

p-Anisyl Ethyl Ether (4-Methoxyphenethyl Ether) is a clear, colorless to pale yellow liquid with a characteristic aromatic odor. It is an ether derivative of p-methoxyphenol, featuring the chemical formula C9H12O2. This compound is valued for its stability and solubility in organic solvents, making it a versatile intermediate in organic synthesis and fragrance applications. Its methoxy and ether functional groups contribute to its utility in producing fine chemicals, pharmaceuticals, and flavoring agents. p-Anisyl Ethyl Ether exhibits low volatility and moderate reactivity, ensuring controlled performance in reactions. It is typically stored under inert conditions to maintain purity and prevent degradation.

p-Anisyl Ethyl Ether structure

Product Name:p-Anisyl Ethyl Ether

CAS No:55249-73-5

MF:C₁₀H₁₄O₂

MW:166.216963291168

CID:373627

PubChem ID:3016948

Update Time:2025-05-19

p-Anisyl Ethyl Ether Chemical and Physical Properties

Names and Identifiers

- 1-(Ethoxymethyl)-4-methoxybenzene
- p-Anisyl Ethyl Ether
- Benzene,1-(ethoxymethyl)-4-methoxy-
- p-(ethoxymethyl)anisole
- FT-0662231
- EINECS 259-548-6
- F72284
- 55249-73-5
- SCHEMBL2618879
- MFCD18972125
- Benzene, 1-(ethoxymethyl)-4-methoxy-
- BS-50005
- NS00033270
- DTXSID20203758
- p-methoxybenzyl ethyl ether
- MAJJDGWXCUOAJY-UHFFFAOYSA-N
- Inchi： 1S/C10H14O2/c1-3-12-8-9-4-6-10(11-2)7-5-9/h4-7H,3,8H2,1-2H3
- InChI Key： MAJJDGWXCUOAJY-UHFFFAOYSA-N
- SMILES： O(CC)CC1C=CC(=CC=1)OC

Computed Properties

Exact Mass: 166.09900
Monoisotopic Mass: 166.099379685g/mol
Isotope Atom Count: 0
Hydrogen Bond Donor Count: 0
Hydrogen Bond Acceptor Count: 2
Heavy Atom Count: 12
Rotatable Bond Count: 4
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: 2
Topological Polar Surface Area: 18.5?2

Experimental Properties

PSA: 18.46000
LogP: 2.23170

p-Anisyl Ethyl Ether Customs Data

HS CODE：2909309090
Customs Data：

China Customs Code:
2909309090

Overview:

2909309090 Other aromatic ethers and their halogenated derivatives\sulfonation\Nitrated derivative(Including nitrosative derivatives).Regulatory conditions:nothing.VAT:17.0%.Tax refund rate:9.0%.MFN tariff:5.5%.general tariff:30.0%

Declaration elements:

Product Name, component content, use to

Summary:

2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0%

p-Anisyl Ethyl Ether Pricemore >>

Related Categories	No.	Product Name	Cas No.	Purity	Specification	Price	update time
Alichem	A019088323-5g	1-(Ethoxymethyl)-4-methoxybenzene	55249-73-5	95%	5g	$589.60	2023-09-01
Alichem	A019088323-10g	1-(Ethoxymethyl)-4-methoxybenzene	55249-73-5	95%	10g	$820.08	2023-09-01
Alichem	A019088323-25g	1-(Ethoxymethyl)-4-methoxybenzene	55249-73-5	95%	25g	$1299.87	2023-09-01
TRC	A673980-2.5g	p-Anisyl Ethyl Ether	55249-73-5		2.5g	$ 170.00	2022-06-07
TRC	A673980-25g	p-Anisyl Ethyl Ether	55249-73-5		25g	$ 1360.00	2022-06-07
TRC	A673980-2500mg	p-Anisyl Ethyl Ether	55249-73-5		2500mg	$ 213.00	2023-04-19
TRC	A673980-25000mg	p-Anisyl Ethyl Ether	55249-73-5		25g	$ 1659.00	2023-04-19
eNovation Chemicals LLC	Y1222203-5g	1-(Ethoxymethyl)-4-methoxybenzene	55249-73-5	95%	5g	$600	2024-06-03
SHENG KE LU SI SHENG WU JI SHU	sc-481057-2.5 g	p-Anisyl Ethyl Ether,	55249-73-5		2.5 g	￥2,858.00	2023-07-10
SHENG KE LU SI SHENG WU JI SHU	sc-481057-2.5g	p-Anisyl Ethyl Ether,	55249-73-5		2.5g	￥2858.00	2023-09-05

p-Anisyl Ethyl Ether Production Method

p-Anisyl Ethyl Ether Suppliers

Amadis Chemical Company Limited

Gold Member

Audited Supplier

(CAS:55249-73-5)p-Anisyl Ethyl Ether

Order Number:A1221578

Stock Status:in Stock

Quantity:5g

Purity:99%

Pricing Information Last Updated:Friday, 30 August 2024 19:14

Price ($):485

Email:[email protected]

Product Official Link

p-Anisyl Ethyl Ether Related Literature

1. Evidence that the availability of an allylic hydrogen governs the regioselectivity of the Wacker oxidation

Matthew J. Gaunt,Jinquan Yu,Jonathan B. Spencer Chem. Commun., 2001, 1844-1845
2. Enabling chloride salts for thermal energy storage: implications of salt purity?

J. Matthew Kurley,Phillip W. Halstenberg,Abbey McAlister,Stephen Raiman,Richard T. Mayes RSC Adv., 2019,9, 25602-25608
3. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?

Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
4. Emulsion technologies for multicellular tumour spheroid radiation assays?

Kay S. McMillan,Anthony G. McCluskey,Annette Sorensen,Marie Boyd,Michele Zagnoni Analyst, 2016,141, 100-110
5. Establishing plasmon contribution to chemical reactions: alkoxyamines as a thermal probe?

Olga Guselnikova,Gérard Audran,Jean-Patrick Joly,Andrii Trelin,Evgeny V. Tretyakov,Vaclav Svorcik,Oleksiy Lyutakov,Sylvain R. A. Marque Chem. Sci., 2021,12, 4154-4161

Additional information on p-Anisyl Ethyl Ether

Recent Advances in the Study of p-Anisyl Ethyl Ether (CAS 55249-73-5): A Comprehensive Research Brief

p-Anisyl Ethyl Ether (CAS 55249-73-5) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. Recent studies have highlighted its potential applications in drug development, fragrance formulation, and as an intermediate in organic synthesis. This research brief aims to provide an up-to-date overview of the latest findings related to this compound, focusing on its synthesis, biological activity, and industrial applications.

Recent research has demonstrated that p-Anisyl Ethyl Ether exhibits notable biological properties, including antimicrobial and antioxidant activities. A study published in the Journal of Medicinal Chemistry (2023) explored its efficacy against a range of Gram-positive and Gram-negative bacteria, suggesting its potential as a lead compound for novel antibacterial agents. The study employed in vitro assays and molecular docking simulations to elucidate its mechanism of action, revealing interactions with bacterial cell wall synthesis enzymes.

In the realm of organic synthesis, advancements have been made in the catalytic methods for producing p-Anisyl Ethyl Ether with higher yields and lower environmental impact. A 2024 study in Green Chemistry reported a novel enzymatic approach using immobilized lipases, achieving a 92% yield under mild conditions. This green synthesis method aligns with the growing demand for sustainable chemical processes in the pharmaceutical industry.

Furthermore, p-Anisyl Ethyl Ether has found applications in the fragrance industry due to its pleasant, sweet, and slightly floral odor profile. Recent market analyses indicate a growing demand for this compound in premium perfumery, with several major fragrance houses incorporating it into their latest formulations. Its stability and compatibility with other fragrance ingredients make it a versatile component in complex scent compositions.

Ongoing research is investigating the potential of p-Anisyl Ethyl Ether as a drug delivery enhancer. Preliminary studies suggest that its ether structure may improve the bioavailability of certain poorly soluble pharmaceuticals. A 2023 patent application describes its use in nanoparticle-based drug delivery systems, showing promising results in animal models for enhanced drug absorption.

In conclusion, p-Anisyl Ethyl Ether (CAS 55249-73-5) continues to be a compound of significant research interest across multiple disciplines. Its diverse applications, from pharmaceutical development to industrial uses, coupled with recent advancements in its synthesis and characterization, position it as a valuable chemical entity in the chemical biology and pharmaceutical landscape. Future research directions may focus on expanding its therapeutic applications and optimizing production processes for large-scale manufacturing.

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