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66667-59-2

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66667-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66667-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,6,6 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66667-59:
(7*6)+(6*6)+(5*6)+(4*6)+(3*7)+(2*5)+(1*9)=172
172 % 10 = 2
So 66667-59-2 is a valid CAS Registry Number.

66667-59-2Relevant articles and documents

Solvent-free synthesis of azomethines, spectral correlations and antimicrobial activities of some E-benzylidene-4-chlorobenzenamines

Suresh,Sakthinathan,Kamalakkannan,Ranganathan,Sathiyamoorthi,Mala,Arulkumaran,Vijayakumar,Sundararajan,Vanangamudi,Subramanian,Thirunarayanan,Vanaja,Kanagambal

, p. 275 - 290 (2015/07/27)

Some azomethines including substituted benzylidene-4-chlorobenzenamines (E-imines) have been synthesized by fly-ash: PTS catalyzed microwave assisted condensation of 4-chloroaniline and substituted benzaldehydes under solvent-free conditions. The yield of the imines has been found to be more than 85%. The purity of all imines has been checked using their physical constants and UV, IR and NMR spectral data. These spectral data have been correlated with Hammett substituent constants and F and R parameters using single and multi-linear regression analysis. From the results of statistical analysis, the effect of substituents on the above spectral data has been studied. The antimicrobial activities of all imines have been studied using standard methods.

Microwave-assisted, solvent-free, parallel syntheses and elucidation of reaction mechanism for the formation of some novel tetraaryl imidazoles of biological interest

Kumar, B. R. Prashantha,Sharma, Gyanendra Kumar,Srinath,Noor, Mohamed,Suresh,Srinivasa

experimental part, p. 278 - 284 (2009/07/05)

The microwave assisted, solvent free, parallel syntheses of title compounds is described in this protocol. Twelve new tetraaryl imidazoles, which are incorporated with the chemotherapeutic pharmaco- phores, have been synthesized by adopting one pot multic

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