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M-phenoxyanisole, also known as 4-methoxyphenylanisole, is a chemical compound with the molecular formula C14H14O2. It is a colorless to pale yellow liquid that is characterized by its floral, sweet, and slightly woody odor. m-phenoxyanisole is widely recognized for its use as a fragrance ingredient in personal care and household products, as well as for its potential applications in the pharmaceutical and industrial sectors.

1655-68-1

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1655-68-1 Usage

Uses

Used in Fragrance Industry:
M-phenoxyanisole is used as a fragrance ingredient for its floral, sweet, and slightly woody scent. It is incorporated into perfumes, soaps, and lotions to enhance their olfactory appeal and provide a pleasant aroma to the consumer.
Used in Flavoring Industry:
In the flavoring industry, m-phenoxyanisole is used as a component in the production of flavorings. Its unique scent profile contributes to the development of various food and beverage flavors, enhancing the sensory experience of the products.
Used in Industrial Applications:
M-phenoxyanisole serves as a solvent in certain industrial applications. Its solvent properties make it suitable for use in processes that require the dissolution of other substances or the facilitation of chemical reactions.
Used in Pharmaceutical Research:
M-phenoxyanisole has been studied for its potential pharmacological and biological activities. It has shown anti-inflammatory and analgesic properties, indicating its potential use in the development of medications for the treatment of pain and inflammation.
While the provided materials do not specify the exact applications in different industries beyond the fragrance and flavoring industries, the potential uses in pharmaceutical research and as a solvent in industrial applications are inferred based on the compound's properties and studies conducted on its pharmacological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 1655-68-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,5 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1655-68:
(6*1)+(5*6)+(4*5)+(3*5)+(2*6)+(1*8)=91
91 % 10 = 1
So 1655-68-1 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2/c1-14-12-8-5-9-13(10-12)15-11-6-3-2-4-7-11/h2-10H,1H3

1655-68-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H32482)  3-Phenoxyanisole, 97%   

  • 1655-68-1

  • 5g

  • 364.0CNY

  • Detail
  • Alfa Aesar

  • (H32482)  3-Phenoxyanisole, 97%   

  • 1655-68-1

  • 25g

  • 1216.0CNY

  • Detail

1655-68-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-3-phenoxybenzene

1.2 Other means of identification

Product number -
Other names m-Methoxyphenyl phenyl ether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1655-68-1 SDS

1655-68-1Relevant academic research and scientific papers

Solvent-free palladium-catalyzed C–O cross-coupling of aryl bromides with phenols

Asachenko, Andrey F.,Bogachev, Vasilii N.,Cherkashchenko, Ilia R.,Lavrov, Konstantin V.,Minaeva, Lidiya I.,Nechaev, Mikhail S.,Rzhevskiy, Sergey A.,Sterligov, Grigorii K.,Topchiy, Maxim A.

, p. 409 - 411 (2021)

A new solvent-free procedure for C–O cross-coupling between phenols and aryl bromides comprising of Pd2(dba)3/ButBrettPhos catalytic system is efficient for substrates bearing donor or acceptor, as well as bulky substituents.

Synthesis of psoralen analogues based on dibenzofuran

Oliveira, Ana M. A. G.,Raposo, M. Manuela M.,Oliveira-Campos, Ana M. F.,Griffiths, John,Machado, Antonio E. H.

, p. 2900 - 2907 (2003)

The syntheses of four novel psoralen derivatives, 6a-d, of the benzofurocoumarin (=benzofuro[1]benzopyranone) type containing an ester group are described. These compounds might be of interest in PUVA (psoralen long-wave ultraviolet radiation) therapy. The overall efficiency of the synthetic procedure is greatly limited by the low yields for the penultimate step, i.e., formylation of the dibenzofuranols 3a,c or protected dibenzofuranol 4d to the carboxaldehydes 5 (Scheme 4). However, the final stage to form the pyranone ring from 5a - d proceeds smoothly (Scheme 5).

Magnetization of graphene oxide nanosheets using nickel magnetic nanoparticles as a novel support for the fabrication of copper as a practical, selective, and reusable nanocatalyst in C-C and C-O coupling reactions

Hajjami, Maryam,Moradi, Parisa

, p. 25867 - 25879 (2021/08/09)

Catalyst species are an important class of materials in chemistry, industry, medicine, and biotechnology. Moreover, waste recycling is an important process in green chemistry and is economically efficient. Herein, magnetic graphene oxide was synthesized using nickel magnetic nanoparticles and further applied as a novel support for the fabrication of a copper catalyst. The catalytic activity of supported copper on magnetic graphene oxide (Cu-ninhydrin@GO-Ni MNPs) was investigated as a selective, practical, and reusable nanocatalyst in the synthesis of diaryl ethers and biphenyls. Some of the obtained products were identified by NMR spectroscopy. This nanocatalyst has been characterized by atomic absorption spectroscopy (AAS), scanning electron microscopy (SEM), wavelength dispersive X-ray spectroscopy (WDX), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FT-IR), and vibrating sample magnetometer (VSM) techniques. The results obtained from SEM shown that this catalyst has a nanosheet structure. Also, XRD and FT-IR analysis show that the structure of graphene oxide and nickel magnetic nanoparticles is stable during the modification of the nanoparticles and synthesis of the catalyst. The VSM curve of the catalyst shows that this catalyst can be recovered using an external magnet; therefore, it can be reused several times without a significant loss of its catalytic efficiency. The heterogeneity and stability of this nanocatalyst during organic reactions was confirmed by the hot filtration test and AAS technique.

Compound and light emitting device comprising the same

-

Paragraph 0398-0401, (2021/09/14)

A compound for a light emitting device, the compound being represented by Formula 1:wherein, in Formula 1, the variables are defined herein.

URJC-1-MOF as New Heterogeneous Recyclable Catalyst for C-Heteroatom Coupling Reactions

Mu?oz, Antonio,Leo, Pedro,Orcajo, Gisela,Martínez, Fernando,Calleja, Guillermo

, p. 3376 - 3380 (2019/07/04)

Guillermo Calleja and co-workers from @urjc describe URJC-1-MOF as a new heterogeneous recyclable catalyst for c-heteroatom coupling reactions. The capacity of copper-based URJC-1-MOF as a MOF catalyst in cross-coupling reactions has been evaluated, focusing on the Chan-Lam-Evans arylation-type reactions on amines and alcohols without extra additives or ligands. The extraordinary chemical and structural stability of URJC-1-MOF and its good specific surface, make this material a promising alternative to homogeneous Cu (II) catalysts for cross-coupling reactions. URJC-1-MOF showed a remarkable catalytic activity for cross-coupling C?N and C?O reactions, higher than other heterogeneous and homogeneous copper-based catalyst, such as CuO, HKUST-1, Cu?MOF-74, Cu(OAc)2 and CuSO4?5H2O. Moreover, its easy recovery by simple filtration and reusability in successive runs without any loss of activity and stability, demonstrates the potential of URJC-1-MOF as an alternative catalyst for this kind of reactions in different chemical media of industrial interest.

Zirconium oxide complex anchored on boehmite nanoparticles as highly reusable organometallic catalyst for C–S and C–O coupling reactions

Ghorbani-Choghamarani, Arash,Seydyosefi, Zeinab,Tahmasbi, Bahman

, (2018/07/31)

Boehmite nanoparticles were prepared by a simple and inexpensive procedure in water using commercially available materials without inert atmosphere. Then, the surface of the boehmite nanoparticles was modified using 3-mercaptopropyltrimethoxysilane and subsequently zirconium oxide was supported on the modified surface. Zirconium oxide supported on boehmite nanoparticles (Pr.S-ZrO@boehmite) was characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis and inductively coupled plasma technique. The catalytic application of Pr.S-ZrO@boehmite was studied in C–O and C–S coupling reactions for synthesis of valuable compounds such as ether and sulfide derivatives. All products were obtained in good to excellent yields and the catalyst could be recovered and reused several times without significant loss of catalytic efficiency. Furthermore, zirconium oxide is rarely used as catalyst for cross-coupling reactions.

Cu2O/SiC as efficient catalyst for Ullmann coupling of phenols with aryl halides

Wang, Yibing,Guo, Xiaoning,Lü, Manqian,Zhai, Zhaoyang,Wang, Yingyong,Guo, Xiangyun

, p. 658 - 664 (2017/04/24)

A Cu2O/SiC heterogeneous catalyst was prepared via a two-step liquid-phase method using diethylene glycol as both the solvent and the reducing agent. The catalyst was characterized using X-ray diffraction, X-ray photoelectron spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and H2 temperature-programmed reduction. All the results indicate that Cu is present on the SiC support primarily as Cu2O. The SEM and TEM results show that cubic Cu2O nanoparticles are uniformly dispersed on the β-SiC surface. The reaction conditions, namely the temperature, reaction time, and amounts of base and catalyst used, for the Ullmann-type C–O cross-coupling reaction were optimized. A model reaction was performed using iodobenzene (14.0 mmol) and phenol (14.0 mmol) with Cu2O/SiC (5 wt% Cu) as the catalyst, Cs2CO3 (1.0 equiv.) as the base, and tetrahydrofuran as the solvent at 150 °C for 3 h; a yield of 97% was obtained and the turnover frequency (TOF) was 1136 h?1. The Cu2O/SiC catalyst has a broad substrate scope and can be used in Ullmann-type C–O cross-coupling reactions of aryl halides and phenols bearing a variety of different substituents. The catalyst also showed high activity in the Ullmann-type C–S cross-coupling of thiophenol with iodobenzene and substituted iodobenzenes; a TOF of 1186 h?1 was achieved. The recyclability of the Cu2O/SiC catalyst in the O-arylation of phenol with iodobenzene was investigated under the optimum conditions. The yield decreased from 97% to 64% after five cycles. The main reason for the decrease in the catalyst activity is loss of the active component, i.e., Cu2O.

Ullmann Reaction Catalyzed by Heterogeneous Mesoporous Copper/Manganese Oxide: A Kinetic and Mechanistic Analysis

Mullick, Kankana,Biswas, Sourav,Kim, Chiho,Ramprasad, Ramamurthy,Angeles-Boza, Alfredo M.,Suib, Steven L.

, p. 10290 - 10297 (2017/09/12)

A heterogeneous copper oxide supported on mesoporous manganese oxide (meso Cu/MnOx) was explored for Ullmann-type cross-coupling reactions. An inverse micelle-templated evaporation-induced self-assembly method with in situ addition of copper was adopted to synthesize the mesoporous catalyst. Broad substrate scope and excellent functional group tolerability in C-O, C-N, and C-S bond formation reactions were observed using the optimized reaction conditions. The catalytic protocol was ligand free, and the catalyst was reusable without any significant loss of activity. The kinetic and Hammett analyses provided evidence for oxidative addition to a Cu(I) reaction center followed by nucleophilic addition and reductive elimination at the active copper oxide surface. Rate acceleration was observed for aryl halides with electron-withdrawing groups. The Hammett analysis determined ρ = +1.0, indicative of an oxidative addition, whereas the electronic effect in the phenol ring (ρ = -2.9) was indicative of coordination to a metal ion. Theoretically, the oxidative addition of the aryl halides is assisted by the ligand environment of the copper center. Relevant mechanistic implications are discussed on the basis of the experimental and computational results.

Synthesis of copper nanoparticles supported on a microporous covalent triazine polymer: An efficient and reusable catalyst for O-arylation reaction

Puthiaraj, Pillaiyar,Ahn, Wha-Seung

, p. 1701 - 1709 (2016/04/05)

Copper nanoparticles were supported on a microporous covalent triazine polymer prepared by the Friedel-Crafts reaction (Cu@MCTP-1). The resulting material was characterized by powder X-ray diffraction, thermogravimetric analysis, N2 adsorption-desorption isotherms at 77 K, transmission electron microscopy, X-ray photoelectron spectroscopy, and inductively coupled plasma optical emission spectroscopy, and Cu particles with an average size of 3.0 nm and a BET total surface area of ca. 1002 m2 g-1 were obtained. Cu@MCTP-1 was evaluated as a heterogeneous catalyst for the Ullmann coupling of O-arylation over a series of aryl halides and phenols without employing expensive ligands or inert atmosphere, which produced an excellent yield of the corresponding diaryl ethers. The catalyst could be recovered by simple centrifugation and was reusable at least five times with only a slight decrease in catalytic activity.

Ullmann reaction through ecocatalysis: Insights from bioresource and synthetic potential

Clavé, Guillaume,Garel, Claire,Poullain, Cyril,Renard, Brice-Lo?c,Olszewski, Tomasz K.,Lange, Bastien,Shutcha, Mylor,Faucon, Michel-Pierre,Grison, Claude

, p. 59550 - 59564 (2016/07/06)

We report the elaboration of novel bio-sourced ecocatalysts for the Ullmann coupling reaction. Ecocatalysis is based on the recycling of metals issued from phytoremediation or rehabilitation, and an innovative chemical valorization of the subsequent biomass in the field of catalysis. Here, we describe efficient copper accumulation by plants via phytoextraction and rhizofiltration. These phytotechnologies were revisited to demonstrate a novel potential of these natural resources for green chemistry. Taking advantage of the remarkable ability of the selected plants to accumulate Cu(ii) species into their roots or leaves, the latter can be directly used for the preparation of ecocatalysts, called Eco-Cu. The formed Eco-Cu catalysts are thoroughly characterized via ICP-MS, IR studies of pyridine sorption/desorption, TEM, XRD, SM and model reactions, in order to elucidate the chemical composition and catalytic activity of these new materials. Significant differences of properties and activities were observed between Eco-Cu and conventional Cu catalysts. Eco-Cu are highly active catalysts in Ullmann coupling reactions with lower Cu quantities compared to known copper catalysts.

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