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2,4-di((2H)-methyl)-6-phenylpyrimidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1356265-33-2

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1356265-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1356265-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,2,6 and 5 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1356265-33:
(9*1)+(8*3)+(7*5)+(6*6)+(5*2)+(4*6)+(3*5)+(2*3)+(1*3)=162
162 % 10 = 2
So 1356265-33-2 is a valid CAS Registry Number.

1356265-33-2Downstream Products

1356265-33-2Relevant academic research and scientific papers

Monitoring mechanistic details in the synthesis of pyrimidines via real-time, ultrafast multidimensional NMR spectroscopy

Pardo, Zulay D.,Olsen, Gregory L.,Fernandez-Valle, Maria Encarnacion,Frydman, Lucio,Martinez-Alvarez, Roberto,Herrera, Antonio

, p. 2706 - 2715 (2012)

Recent years have witnessed unprecedented advances in the development of fast multidimensional NMR acquisition techniques. This progress could open valuable new opportunities for the elucidation of chemical and biochemical processes. This study demonstrates one such capability, with the first real-time Two-dimensional (2D) dynamic analysis of a complex organic reaction relying on unlabeled substrates. Implementing such measurements required the development of new ultrafast 2D methods, capable of monitoring multiple spectral regions of interest as the reaction progressed. The alternate application of these acquisitions in an interleaved, excitation-optimized fashion, allowed us to extract new structural and dynamic insight concerning the reaction between aliphatic ketones and triflic anhydride in the presence of nitriles to yield alkylpyrimidines. Up to 2500 2D NMR data sets were thus collected over the course of this nearly 100 min long reaction, in an approach resembling that used in functional magnetic resonance imaging. With the aid of these new frequency-selective low-gradient strength experiments, supplemented by chemical shift calculations of the spectral coordinates observed in the 2D heteronuclear correlations, previously postulated intermediates involved in the alkylpyrimidine formation process could be confirmed, and hitherto undetected ones were revealed. The potential and limitations of the resulting methods are discussed.

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