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1-Propanone, 1-(4-methoxyphenyl)-3-(1-piperidinyl)- is a complex organic compound with the molecular formula C16H23NO2. It is a derivative of propanone, featuring a 4-methoxyphenyl group attached to the first carbon and a piperidinyl group attached to the third carbon. 1-Propanone, 1-(4-methoxyphenyl)-3-(1-piperidinyl)- is characterized by its unique structure, which combines the properties of a ketone, an ether, and a piperidine ring. It is likely to be found in research settings, particularly in the fields of medicinal chemistry and material science, where its specific chemical properties and potential applications are explored. Due to its complex structure, it may have specific interactions with biological systems or be used in the synthesis of more complex molecules.

1219-34-7

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1219-34-7 Usage

Chemical class

Aryl ketones

Usage

Building block or intermediate in the synthesis of various compounds in research and pharmaceutical industries

Characterized by

Aromatic and ketonic moieties, as well as a piperidine ring

Versatility

Potential applications in drug discovery and development

Pharmacological properties

Of interest to scientists and researchers in the field of medicinal chemistry and CNS drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 1219-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1219-34:
(6*1)+(5*2)+(4*1)+(3*9)+(2*3)+(1*4)=57
57 % 10 = 7
So 1219-34-7 is a valid CAS Registry Number.

1219-34-7Relevant academic research and scientific papers

Continuous Flow Acylation of (Hetero)aryllithiums with Polyfunctional N,N-Dimethylamides and Tetramethylurea in Toluene

Djukanovic, Dimitrije,Filipponi, Paolo,Heinz, Benjamin,Knochel, Paul,Mandrelli, Francesca,Martin, Benjamin,Mostarda, Serena

supporting information, p. 13977 - 13981 (2021/09/13)

The continuous flow reaction of various aryl or heteroaryl bromides in toluene in the presence of THF (1.0 equiv) with sec-BuLi (1.1 equiv) provided at 25 °C within 40 sec the corresponding aryllithiums which were acylated with various functionalized N,N-

Identification of dual Sigma1 receptor modulators/acetylcholinesterase inhibitors with antioxidant and neurotrophic properties, as neuroprotective agents

Rui, Marta,Rossino, Giacomo,Coniglio, Stefania,Monteleone, Stefania,Scuteri, Arianna,Malacrida, Alessio,Rossi, Daniela,Catenacci, Laura,Sorrenti, Milena,Paolillo, Mayra,Curti, Daniela,Venturini, Letizia,Schepmann, Dirk,Wünsch, Bernhard,Liedl, Klaus R.,Cavaletti, Guido,Pace, Vittorio,Urban, Ernst,Collina, Simona

, p. 353 - 370 (2018/09/21)

In this manuscript we report on the design, synthesis and evaluation of dual Sigma 1 Receptor (S1R) modulators/Acetylcholinesterase (AChE) inhibitors endowed with antioxidant and neurotrophic properties, potentially able to counteract neurodegeneration. The compounds based on arylalkylaminoketone scaffold integrate the pharmacophoric elements of RRC-33, a S1R modulator developed by us, donepezil, a well-known AChE inhibitor, and curcumin, a natural antioxidant compound with neuroprotective properties. A small library of compounds was synthesized and preliminary in vitro screening performed. Some compounds showed good S1R binding affinity, selectivity towards S2R and N-Methyl-D-Aspartate (NMDA) receptor, AChE relevant inhibiting activity and are potentially able to bypass the BBB, as predicted by the in silico study. For the hits 10 and 20, the antioxidant profile was assessed in SH-SY5Y human neuroblastoma cell lines by evaluating their protective effect against H2O2 cytotoxicity and reactive oxygen species (ROS) production. Tested compounds resulted effective in decreasing ROS production, thus ameliorating the cellular survival. Moreover, compounds 10 and 20 showed to be effective in promoting the neurite elongation of Dorsal Root Ganglia (DRG), thus demonstrating a promising neurotrophic activity. Of note, the tested compounds did not show any cytotoxic effect at the concentration assayed. Relying on these encouraging results, both compounds will undergo a structure optimization program for the development of therapeutic candidates for neurodegenerative diseases treatment.

An umpolung strategy for the synthesis of β-aminoketones via copper-catalyzed electrophilic amination of cyclopropanols

Ye, Zhishi,Dai, Mingji

supporting information, p. 2190 - 2193 (2015/05/13)

A novel copper-catalyzed electrophilic amination of cyclopropanols with O-benzoyl-N,N-dialkylhydroxylamines to synthesize various β-aminoketones via a sequence that includes C-C bond cleavage and Csp3-N bond formation is reported. The reaction conditions are mild and tolerate a wide range of functional groups including benzoate, tosylate, expoxide, and α,β-unsaturated carbonyls, which are incompatible in the traditional amine nucleophilic conjugate addition and the Mannich reaction conditions. Preliminary mechanistic studies and a proposed catalytic cycle of this umpolung β-aminoketone synthesis process have been described as well.

EFFECT OF THE STRUCTURE OF THE REAGENTS ON THE FORMATION RATE OF ARYL VINYL KETONES IN THE REACTION OF AMINES WITH β-HALOGENOPROPIOPHENONES

Popov, A. F.,Piskunova, Zh. P.,Matvienko, V. N.

, p. 1918 - 1921 (2007/10/02)

The dependence of the formation rate of aryl vinyl ketones in the reaction of ring-substituted β-halogenopropiophenones with various amines on the structure of the reagents was investigated.By analysis of the obtained data it was concluded that the process takes place by an E2 mechanism through an anion-like transition state.

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