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N,N'-(1,3-phenylenebis(methan-1-yl-1-ylidene))dianiline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

16742-78-2

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16742-78-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16742-78-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,7,4 and 2 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16742-78:
(7*1)+(6*6)+(5*7)+(4*4)+(3*2)+(2*7)+(1*8)=122
122 % 10 = 2
So 16742-78-2 is a valid CAS Registry Number.

16742-78-2Downstream Products

16742-78-2Relevant academic research and scientific papers

Exploration of imidazole and imidazopyridine dimers as anticancer agents: Design, synthesis, and structure–activity relationship study

Meenakshisundaram, Sangeetha,Manickam, Manoj,Pillaiyar, Thanigaimalai

, (2019/11/03)

Dimerization of proteins/receptors plays a critical role in various cellular processes, including cell proliferation and differentiation. Therefore, targeting such dimeric proteins/receptors by dimeric small molecules could be a potential therapeutic appr

Synthesis of bistetrahydroquinolines as potential anticholinesterasic agents by double diels-alder reactions

Duarte, Yorley,Gutierrez, Margarita,Astudillo, Luis,Alzate-Morales, Jans,Valdes, Natalia

, p. 12951 - 12965 (2013/11/06)

The tetrahydroquinoline ring system is a unit found in many biologically active natural products and pharmacologically relevant therapeutic agents. A new series of bistetrahydroquinolines (bis-THQs) was synthesized using imino Diels-Alder reactions betwee

Parallel Recognition by Kinetic Control with Imino Aldehyde Substrates that are Prone to Redistribution

Orita, Akihiro,Nagano, Yoshifumi,Nakazawa, Koichi,Otera, Junzo

, p. 548 - 555 (2007/10/03)

One-shot treatment of a mixture of Danishefsky diene 4 and tetraallyltin 8 with 3-formylbenzylidene imines 1 in the presence of Sc(OTf)3 catalyst provides a single product 13 as a result of exclusive Diels-Alder and allylation reactions on the imine and aldehyde functions, respectively. The chemoselectivities of the respective elementary reactions are improved in the parallel reaction, and the redistribution of substrate 1 that is induced readily by Sc(OTf)3 is completely suppressed, thus offering a novel protocol for simplification of the multi-step chemical process.

SYNTHESIS, NMR INVESTIGATION AND FAB-MS CHARACTERIZATION OF 1-AMINO-2-ARYLMETHYL-DIPHOSPHONATE ESTERS

Failla, Salvatore,Finocchiaro, Paolo,Hagele, Gerhard,Rapisardi, Roberto

, p. 79 - 90 (2007/10/02)

Variously substituted amino aryl-methyl-diphosphonate ethyl esters have been prepared in good yields by adding diethyl phosphonate to the corresponding Schiff bases.All compounds were characterized by NMR and MS-FAB techniques, which reveal the presence o

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