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2-(3-methoxyphenyl)propanoic acid, commonly known as ibuprofen, is a nonsteroidal anti-inflammatory drug (NSAID) that exhibits anti-inflammatory, analgesic, and antipyretic properties. It functions by inhibiting the production of prostaglandins, which are chemicals responsible for inflammation, pain, and fever. Ibuprofen is available over-the-counter and can be prescribed in higher doses for more severe conditions. While generally safe when used as directed, long-term or high-dose use may lead to side effects such as stomach irritation, heartburn, and an increased risk of heart attack or stroke.

3146-60-9

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3146-60-9 Usage

Uses

Used in Pharmaceutical Industry:
2-(3-methoxyphenyl)propanoic acid is used as an analgesic for relieving mild to moderate pain, such as headaches, toothaches, and menstrual cramps.
2-(3-methoxyphenyl)propanoic acid is used as an anti-inflammatory agent for treating inflammation associated with conditions like arthritis and soft tissue injuries.
2-(3-methoxyphenyl)propanoic acid is used as an antipyretic to reduce fever in cases of minor infections or other causes.
Used in Over-the-Counter Medications:
2-(3-methoxyphenyl)propanoic acid is used as an active ingredient in various over-the-counter pain relief and fever reduction formulations, providing quick and accessible relief for consumers.
Used in Prescription Medicines:
For more severe pain and inflammation, 2-(3-methoxyphenyl)propanoic acid is used in prescription-strength formulations, allowing for targeted and effective treatment under medical supervision.

Check Digit Verification of cas no

The CAS Registry Mumber 3146-60-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,4 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3146-60:
(6*3)+(5*1)+(4*4)+(3*6)+(2*6)+(1*0)=69
69 % 10 = 9
So 3146-60-9 is a valid CAS Registry Number.

3146-60-9Relevant academic research and scientific papers

Site-Selective, Remote sp3 C?H Carboxylation Enabled by the Merger of Photoredox and Nickel Catalysis

Sahoo, Basudev,Bellotti, Peter,Juliá-Hernández, Francisco,Meng, Qing-Yuan,Crespi, Stefano,K?nig, Burkhard,Martin, Ruben

supporting information, p. 9001 - 9005 (2019/06/24)

A photoinduced carboxylation of alkyl halides with CO2 at remote sp3 C?H sites enabled by the merger of photoredox and Ni catalysis is described. This protocol features a predictable reactivity and site selectivity that can be modulated by the ligand backbone. Preliminary studies reinforce a rationale based on a dynamic displacement of the catalyst throughout the alkyl side chain.

Regioselectivity inversion tuned by iron(iii) salts in palladium-catalyzed carbonylations

Huang, Zijun,Cheng, Yazhe,Chen, Xipeng,Wang, Hui-Fang,Du, Chen-Xia,Li, Yuehui

supporting information, p. 3967 - 3970 (2018/04/23)

Impactful regioselectivity control is crucial for cost-effective chemical synthesis. By using cheap and abundant iron(iii) salts, the hydroxycarbonylations of both aromatic and aliphatic alkenes were significantly enhanced in both reactivity and selectivity (iso/n or n/iso up to >99:1). Moreover, Pd-catalyzed carbonylation selectivity can be switched from branched to linear by using different Fe(iii) salts. In addition, similar results were obtained for the carbonylation of secondary alcohols.

Ligand-Controlled Regioselective Hydrocarboxylation of Styrenes with CO2 by Combining Visible Light and Nickel Catalysis

Meng, Qing-Yuan,Wang, Shun,Huff, Gregory S.,Konig, Burkhard

supporting information, p. 3198 - 3201 (2018/03/13)

The ligand-controlled Markovnikov and anti-Markovnikov hydrocarboxylation of styrenes with atmospheric pressure of CO2 at room temperature using dual visible-light-nickel catalysis has been developed. In the presence of neocuproine as ligand, the Markovnikov product is obtained exclusively, while employing 1,4-bis(diphenylphosphino)butane (dppb) as the ligand favors the formation of the anti-Markovnikov product. A range of functional groups and electron-poor, -neutral, as well as electron-rich styrene derivatives are tolerated by the reaction, providing the desired products in moderate to good yields. Preliminary mechanistic investigations indicate the generation of a nickel hydride (H-NiII) intermediate, which subsequently adds irreversibly to styrenes.

A Ligand-Directed Catalytic Regioselective Hydrocarboxylation of Aryl Olefins with Pd and Formic Acid

Liu, Wei,Ren, Wenlong,Li, Jingfu,Shi, Yuan,Chang, Wenju,Shi, Yian

supporting information, p. 1748 - 1751 (2017/04/11)

An effective Pd-catalyzed hydrocarboxylation of aryl olefins with Ac2O and formic acid is described. A variety of 2- and 3-arylpropanoic acids can be regioselectively formed by the judicious choice of ligand without the use of toxic CO gas.

Nickel-Catalyzed Carboxylation of Benzylic C-N Bonds with CO2

Moragas, Toni,Gaydou, Morgane,Martin, Ruben

supporting information, p. 5053 - 5057 (2016/04/26)

A user-friendly Ni-catalyzed reductive carboxylation of benzylic C-N bonds with CO2 is described. This procedure outperforms state-of-the-art techniques for the carboxylation of benzyl electrophiles by avoiding commonly observed parasitic pathways, such as homodimerization or β-hydride elimination, thus leading to new knowledge in cross-electrophile reactions.

Cp2TiCl2-Catalyzed Regioselective Hydrocarboxylation of Alkenes with CO2

Shao, Peng,Wang, Sheng,Chen, Chao,Xi, Chanjuan

supporting information, p. 2050 - 2053 (2016/06/01)

Cp2TiCl2-catalyzed regioselective hydrocarboxylation of alkenes with CO2 to give carboxylic acids in high yields has been developed in the presence of iPrMgCl. The reaction proceeds with a wide range of alkenes under mild conditions. Styrene and its derivatives can transform to α-aryl carboxylic acids, and aliphatic alkenes can transform to form alkanoic acids.

A versatile synthesis of O-desmethylangolensin analogues from methoxy-substituted benzoic acids

Hong, Hyo Jeong,Lee, Jae In

, p. 569 - 574 (2015/02/05)

The synthesis of O-desmethylangolensin (O-DMA) analogues from methoxy-substituted benzoic acids was described. Treatment of methoxy-substituted benzoic acids with 2 equiv of ethyllithium afforded methoxypropiophenones, which were subsequently transformed to ethyl 2-(methoxyphenyl)propionates via 1,2-rearrangement of the methoxyphenyl group using Pb(OAc)4/HClO4 in triethyl orthoformate. After hydrolysis with KOH, the 2-(methoxyphenyl)propionic acids were reacted with di- 2-pyridyl carbonate to afford 2-pyridyl 2-(methoxyphenyl)propionates, which were acylated with methoxy-substituted phenylmagnesium bromides to give methoxy-α-methyldesoxybenzoins. The methoxy groups of these compounds were selectively or fully demethylated using boron tribromide to give diverse O-DMA analogues in high yields.

Iron-catalyzed, highly regioselective synthesis of α-aryl carboxylic acids from styrene derivatives and CO2

Greenhalgh, Mark D.,Thomas, Stephen P.

, p. 11900 - 11903 (2012/09/07)

The iron-catalyzed hydrocarboxylation of aryl alkenes has been developed using a highly active bench-stable iron(II) precatalyst to give α-aryl carboxylic acids in excellent yields and with near-perfect regioselectivity. Using just 1 mol % FeCl2, bis(imino)pyridine 6 (1 mol %), CO 2 (atmospheric pressure), and a hydride source (EtMgBr, 1.2 equiv), a range of sterically and electronically differentiated aryl alkenes were transformed to the corresponding α-aryl carboxylic acids (up to 96% isolated yield). The catalyst was found to be equally active with a loading of 0.1 mol %. Preliminary mechanistic investigations show that an iron-catalyzed hydrometalation is followed by transmetalation and reaction with the electrophile (CO2).

CYCLIC DIARYL ETHER COMPOUNDS AS ANTAGONISTS OF PROSTAGLANDIN D2 RECEPTORS

-

Page/Page column 108, (2009/10/09)

Described herein are compounds that are antagonists of PGD2 receptors. Also described are pharmaceutical compositions and medicaments that include the antagonists of PGD2 receptors described herein, as well as methods of using such antagonists of PGD2 receptors, alone and in combination with other compounds, for treating respiratory, cardiovascular, and other PGD2-dependent or PGD2-mediated conditions or diseases.

Nickel-catalyzed reductive carboxylation of styrenes using CO2

Williams, Catherine M.,Johnson, Jeffrey B.,Rovis, Tomislav

supporting information; experimental part, p. 14936 - 14937 (2009/03/12)

A nickel-catalyzed reductive carboxylation of styrenes using CO2 has been developed. The reaction proceeds under mild conditions using diethylzinc as the reductant. Preliminary data suggests the mechanism involves two discrete nickel-mediated catalytic cycles, the first involving a catalyzed hydrozincation of the alkene followed by a second, slower nickel-catalyzed carboxylation of the in situ formed organozinc reagent. Importantly, the catalyst system is very robust and will fixate CO2 in good yield even if exposed to only an equimolar amount introduced into the headspace above the reaction. Copyright

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