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2-Pyrimidinamine, N-methyl-4,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

66849-37-4

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66849-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66849-37-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,8,4 and 9 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66849-37:
(7*6)+(6*6)+(5*8)+(4*4)+(3*9)+(2*3)+(1*7)=174
174 % 10 = 4
So 66849-37-4 is a valid CAS Registry Number.

66849-37-4Downstream Products

66849-37-4Relevant academic research and scientific papers

SYNTHESIS OF PYRIMIDINE DERIVATIVES BY REACTION OF PYRYLIUM SALTS WITH GUANIDINE AND COMPOUNDS OF THE GUANIDINE SERIES

Zvezdina, E. A.,Zhdanova, M. P.,Dorofeenko, G. N.

, p. 574 - 578 (1980)

2,4,6-Triphenylpyrylium perchlorate reacts with methylguanidine to give 1-methyl-2-amino-4,6-diphenylpyrimidinium perchlorate, which undergoes the Dimroth rearrangement to give 2-methylamino-4,6-diphenylpyrimidine. 2,4,6-Triarylpyrylium perchlorates react

Flow reactor approach for the facile and continuous synthesis of efficient Pd@Pt core-shell nanoparticles for acceptorless dehydrogenative synthesis of pyrimidines from alcohols and amidines

Poly, Sharmin Sultana,Hashiguchi, Yuta,Sultana, Asima,Nakamura, Isao,Shimizu, Ken-ichi,Yasumura, Shunsaku,Fujitani, Tadahiro

, (2021/04/23)

Carbon supported Pd@Pt core-shell nanoparticles catalyst was prepared in a flow reactor toachieve enhanced catalytic activities with low Pt loading for the acceptorless dehydrogenative synthesis of pyrimidines. Spectroscopic (XAS analysis) and microscopic (HAADF-STEM) techniques reveled that the core-shell structure was formed by the applied preparation method. The Pd@Pt/PVP (polyvinylpyrrolidone)/C catalyst showed the activity for the three component one pot synthesis of pyrimidines through a series of consecutive reactions including oxidation of alcohols, C[sbnd]C, and C[sbnd]N coupling, followed by heterocyclization and dehydrogenation employing various primary alcohols, secondary alcohols, and amidines. The reaction mechanism on Pd@Pt/PVP/C catalyst was explored by comparison with the control experiments.

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