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Urea, N-methyl-N-phenyl-N'-2-pyridinyl, also known as 1-Methyl-3-phenyl-5-(2-pyridyl)-1,3,5-triazine-2,4,6-triamine, is an organic compound with the chemical formula C12H13N5. It is a derivative of urea, featuring a triazine ring structure with a methyl group, a phenyl group, and a pyridinyl group attached to the nitrogen atoms. Urea, N-methyl-N-phenyl-N'-2-pyridinyl- is of interest in chemical research and has potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a series of chemical reactions and is characterized by its molecular weight, melting point, and solubility properties.

71344-20-2

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71344-20-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71344-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,3,4 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71344-20:
(7*7)+(6*1)+(5*3)+(4*4)+(3*4)+(2*2)+(1*0)=102
102 % 10 = 2
So 71344-20-2 is a valid CAS Registry Number.

71344-20-2Downstream Products

71344-20-2Relevant academic research and scientific papers

Photocleavage of pyridyl-based aromatic polyureas

Mwaura, Jeremiah,Yang, Baocheng,Li, Rongfu,Morton, Martha,Papadimitrakopoulos, Fotios

, p. 9775 - 9783 (2007/10/03)

The photophysical properties of a metal chelating pyridyl-based aromatic ureas and poly-(1,4-phenylene-2,6-pyridylurea) were investigated. In their solution state and upon exposure to 365 nm UV radiation, these low and high molecular weight compounds were found to cleave the urea linkage nearly quantitatively, generating the corresponding amine-terminated subunits and CO2. Through a series of model compounds along with nuclear magnetic resonance (NMR), UV/vis absorption, and fluorescence spectroscopy characterization, the photocleavage process was delinated as a function of UV dose, O2, and water. The presence of water was found crucial to this photocleavage process with O2 playing a role only in subsequent oxidation of resulting amine functionalities. The experimental results support a light-assisted hydrolysis of the urea bond as the most plausible photocleavage mechanism. The photocleavage of such pyridyl-based ureas can potentially find usages in light-assisted base generation and/or for releasing metal cations.

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