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5-(4'-nitrophenyl)-1,3-diphenyl-1,2,4-triazole is a complex organic compound with the molecular formula C19H14N4O2. It is characterized by a triazole ring system, which is a five-membered ring containing three nitrogen atoms and two carbon atoms. The compound features a 4-nitrophenyl group attached to the 5-position of the triazole ring, and two phenyl groups are connected to the 1 and 3 positions of the triazole. This chemical is often used as a building block in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is also known for its potential applications in materials science, particularly in the development of new dyes and pigments. The compound's properties, such as its stability and solubility, make it a valuable intermediate in organic synthesis.

1051-58-7

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1051-58-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1051-58-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,5 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1051-58:
(6*1)+(5*0)+(4*5)+(3*1)+(2*5)+(1*8)=47
47 % 10 = 7
So 1051-58-7 is a valid CAS Registry Number.

1051-58-7Downstream Products

1051-58-7Relevant academic research and scientific papers

1,3-DIPOLAR CYCLOADDITIONS OF 1-(N-ARYLIDENE)AMINO-1,2,3-TRIAZOLES WITH DIPHENYLNITRILIMINE

Bojilova, Anka,Rodios, Nestor A.,Alexandrou, Nicholas E.

, p. 3233 - 3238 (2007/10/02)

1-(N-arylidene)amino-1,2,3-triazoles (1) and (9) react with diphenylnitrilimine (2) to give the corresponding 1,2,3- and 1,2,4-triazoles (3) and (4) as well as 1- and 2-benzohydrazonoyl-1,2,3-triazoles (5), (10) and (6) and (11) respectively.These products are formed assuming an initial cycloadduct, (7), which upon elimination of the triazole ring gives compounds (3) and (4).Further reaction of the triazole system with (2) gives the hydrazone derivatives (5), (6), (10), and (11).The reaction is also studied on the basis of frontier molecular orbitals (FMO) of the reacting species.

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