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1,4,5-triphenyl-1H-imidazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15033-43-9

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15033-43-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15033-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,3 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 15033-43:
(7*1)+(6*5)+(5*0)+(4*3)+(3*3)+(2*4)+(1*3)=69
69 % 10 = 9
So 15033-43-9 is a valid CAS Registry Number.

15033-43-9Downstream Products

15033-43-9Relevant academic research and scientific papers

Selective synthesis of 1,4,5-trisubstituted imidazoles from α-imino ketones prepared by N-heterocyclic-carbene-catalyzed aroylation

Takashima, Ryo,Tsunekawa, Kaoru,Shinozaki, Maki,Suzuki, Yumiko

, p. 2261 - 2267 (2018/04/02)

An alternative synthetic route to 1,4,5-trisubstituted imidazoles from α-imino ketone, which can be prepared from imidoyl chlorides and aromatic aldehydes via N-heterocycle carbene-catalyzed aroylation was developed. This methodology consists of simple tr

Metal-free, acid-promoted synthesis of imidazole derivatives via a multicomponent reaction

Chen, Chung-Yu,Hu, Wan-Ping,Yan, Pi-Cheng,Senadi, Gopal Chandru,Wang, Jeh-Jeng

supporting information, p. 6116 - 6119 (2014/01/17)

An expedient and metal-free synthetic route has been developed for the construction of tri- and tetrasubstituted imidazole derivatives via acid promoted multicomponent reaction methodology. The reaction proceeded smoothly with a range of functionalities to produce the imidazole scaffolds in good to excellent yields.

Syntheses of imidazoles and pyrroles: Betmic and tosmic as complementary reagents

Katritzky, Alan R.,Cheng, Dai,Musgrave, Richard P.

, p. 67 - 70 (2007/10/03)

p-Tolylsulfonylmethyl isocyanide (TosMIC) and benzotriazol-1-yl-methyl isocyanide (BetMIC) were compared as to their synthetic utilities for the synthesis of imidazoles and pyrroles and found to be complementary.

4,5-DIPHENYLIMIDAZOLES FROM THE CYCLIZATION OF BENZIL N-ALKYLMONOHYDRAZONES

Collibee, William L.,Anselme, Jean-Pierre

, p. 655 - 662 (2007/10/02)

The thermal cyclization of monodisubstituted hydrazones (1) affords the corresponding N-substituted-4,5-diphenylimidazoles in good to excellent yields; possible mechanisms for this unusual cyclization are presented.

THE UNUSUAL CYCLIZATION OF BENZIL MONOHYDRAZONES TO 4,5-DIPHENYLIMIDAZOLES

Collibee, William L.,Anselme, Jean-Pierre

, p. 1595 - 1596 (2007/10/02)

Benzil monodisubstituted hydrazones (2) have been shown to undergo cyclodehydration to the corresponding imidazoles (10) and not to pyrazoles as previously reported.

The Copper-Catalysed Reaction of 2-Chloroimidazoles and 2-Chlorobenzimidazoles with Dimethylamine

Whittle, Chrostopher P.

, p. 1545 - 1551 (2007/10/02)

The preparation of 2-dimethylamino-benzimidazoles and -imidazoles from the corresponding 2-chloro compounds by reaction with dimethylamine is assisted by the presence of copper salts.In the absence of a copper catalyst, 2-chloroimidazoles fail to react.Ki

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