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20374-45-2

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20374-45-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20374-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,3,7 and 4 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20374-45:
(7*2)+(6*0)+(5*3)+(4*7)+(3*4)+(2*4)+(1*5)=82
82 % 10 = 2
So 20374-45-2 is a valid CAS Registry Number.

20374-45-2Downstream Products

20374-45-2Relevant academic research and scientific papers

Knoevenagel condensation in heterogeneous phase catalyzed by IR radiation and Tonsil Actisil FF

Obrador, Esteban,Castro, Martin,Tamariz, Joaquin,Zepeda, Gerardo,Miranda, Rene,Delgado, Francisco

, p. 4649 - 4663 (2007/10/03)

Infrared radiation promoted the synthesis of benzylidenemalononitriles, benzylidenecyanoacetamides and benzylidenecyanoacetic acids by condensation of aromatic aldehydes with the corresponding active methylene compound in the presence of Tonsil Actisil FF, without solvent. Mass of catalyst, solvent, and reaction time were assessed in order to improve the efficiency of this process.

Tyrphostins I: Synthesis and Biological Activity of Protein Tyrosine Kinase Inhibitors

Gazit, Aviv,Yaish, Pnina,Gilon, Chaim,Levitzki, Alexander

, p. 2344 - 2352 (2007/10/02)

A novel class of low molecular weight proteine kinase inhibitors is described.These compounds consitute a systematic series of molecules with a progressive increase in affinity toward the substrate site of the EGF receptor kinase domain.These competitive inhibitors also effectively block the EGF-dependent autophosphorylation of the receptor.The potent EGF receptor kinase blockers examined were found to competitively inhibit the homologous insulin receptor kinase at 102-103 higher inhibitor concentrations in spite of the significant homology between these protein tyrosine kinases.These results demonstrate the ability to synthesize selective tyrosine kinase inhibitors.The most potent EGF receptor kinase inhibitors also inhibit the EGF-dependent proliferation of A431/clone 15 cells with little or no effect on EGF independent cell growth.These results demonstrate the potential use of protein tyrosine kinase inhibitors as selective antiproliferative agents for proliferative diseases caused by the hyperactivity of protein tyrosine kinases.We have suggested the name "tyrphostins" for this class of antiproliferative compounds which act as protein tyrosine kinase blockers.

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