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1H-Imidazole, 1-(1-phenylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60197-34-4

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60197-34-4 Usage

Structure

A substituted imidazole derivative with a phenylethyl group attached to the nitrogen atom

Usage

Commonly used as a building block in the synthesis of pharmaceuticals and biologically active molecules

Therapeutic applications

Studied for its potential as an antifungal agent and as a modulator of various physiological processes

Other potential uses

Investigated for its potential use in organic synthesis and as a ligand in coordination chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 60197-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,9 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 60197-34:
(7*6)+(6*0)+(5*1)+(4*9)+(3*7)+(2*3)+(1*4)=114
114 % 10 = 4
So 60197-34-4 is a valid CAS Registry Number.

60197-34-4Relevant academic research and scientific papers

Remarkable improvement achieved by imidazole derivatives in ruthenium-catalyzed hydroesterification of alkenes using formates

Konishi, Hideyuki,Muto, Takashi,Manabe, Kei,Ueda, Tsuyoshi

supporting information, p. 4722 - 4725,4 (2012/12/12)

Imidazole derivatives are revealed to be effective ligands in the Ru-catalyzed hydroesterification of alkenes using formates, affording one-carbonelongated esters in high yields. Further, intramolecular hydroesterification was successfully performed to give lactones for the first time. Imidazole derivatives can contribute to promote the reaction as well as to suppress the undesired decarbonylation of formate. Toxic CO gas, a directing group, and large excess alkenes are not required.

Bridged imidazolium salts used as precursors for chelating carbene complexes of palladium in the Mizoroki-Heck reaction

Scherg, Tobias,Schneider, Sabine K.,Frey, Guido D.,Schwarz, Jürgen,Herdtweck, Eberhardt,Herrmann, Wolfgang A.

, p. 2894 - 2907 (2008/03/13)

A variety of chiral and achiral imidazolium salts is synthesized. Methylene-, ethylene-, propylene- and pyridinyl-bridged bis(imidazolium) halides are used to generate the respective free chelating carbenes. The synthesis of palladium complexes of general formula [cis-CH2{NC(H)=C(H)N(R)C} 2PdX2] with these chelating N-heterocyclic carbene ligands is reported. Structural proofs of complexes 28 and 46 are represented by X-ray diffraction studies. Catalytic applications in the Mizoroki-Heck reaction are presented. Georg Thieme Verlag Stuttgart.

The reaction of carbonyldiimidazole with alcohols to form carbamates and N-alkylimidazoles

Tang, Yuanqing,Dong, Yuxiang,Vennerstrom, Jonathan L.

, p. 2540 - 2544 (2007/10/03)

The reactions of non-benzylic primary and secondary aliphatic alcohols with carbonyldiimidazole (CDI) afford the corresponding carbamates but not N-alkylimidazoles. For benzylic primary alcohols, formation of N-alkylimidazoles proceeds reasonably at 170 °C in several different solvents and occurs by way of the initially formed carbamate. However, under these rather forcing conditions, or even at lower reaction temperatures, elimination is a significant side reaction for benzylic secondary alcohols with β-hydrogen atoms. With one exception, reactions of six N,N-disubstituted β-aminoalcohols with CDI to form N-alkylimidazoles proceed under relatively mild conditions and may occur by way of an aziridinium intermediate.

Dicationic electrophiles from olefinic amines in superacid

Zhang, Yun,McElrea, Aaron,Sanchez Jr., Gregorio V.,Do, Dat,Gomez, Alma,Aguirre, Sharon L.,Rendy, Rendy,Klumpp, Douglas A.

, p. 5119 - 5122 (2007/10/03)

This paper describes the superacid-catalyzed chemistry of olefinic amines and related compounds. A variety of olefinic amines are found to react with benzene in CF3SO3H (triflic acid) to give addition products in good yields (75-99%), including the pharmaceutical agents fenpiprane and prozapine. A general mechanism is proposed that invokes the formation of reactive, dicationic electrophiles and the direct observation of a diprotonated species is reported from low-temperature NMR experiments. This chemistry is also used to conveniently prepare functionalized polystyrene beads having pendant amine groups.

Influence of some novel N-substituted azoles and pyridines on rat hepatic CYP3A activity

Slama, James T.,Hancock, Julie L.,Rho, Taikyun,Sambucetti, Lidia,Bachmann, Kenneth A.

, p. 1881 - 1892 (2008/04/18)

A series of N-substituted heteroaromatic compounds structurally related to clotrimazole was synthesized, and the effects of these compounds on ethosuximide clearance in rats were determined as a measure of their abilities to induce cytochrome P4503A (CYP3A) activity. Ethosuximide clearance and in vitro erythromycin N-demethylase activity were shown to correlate. In this series, imidazole or other related heteroaromatic 'head groups' were linked to triphenylmethane or other phenylmethane derivatives. Within the series, it was found that 1-triphenylmethane-substituted imidazoles elicited the greatest increase in CYP3A activity, and that among the triphenylmethyl-substituted imidazoles, the highest activities were achieved by the substitution of F- or Cl- in either the meta or para position of one of the phenyl rings. Diphenylmethylsubstituted pyridine was effectively devoid of activity. Compounds eliciting the largest increase in CYP3A activity (viz. 1-[(3-fluorophenyl)diphenylmethyl]imidazole, 1-[(4- fluorophenyl)diphenylmethyl]imidazole, and 1-[tri-(4- fluorophenyl)methyl]imidazole) produced little or no increase in ethoxyresorufin O-dealkylase (EROD) activity (i.e. CYP1A), whereas benzylimidazole, which elicited only a small increase in CYP3A activity, produced an almost 9-fold increase in CYP1A activity. For a series of eleven compounds exhibiting a wide range of influence on CYP3A activity, a positive correlation was found between ethosuximide clearance and hepatic CYP3A mRNA levels.

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