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5-(m-nitrophenyl)-1H-1,2,4-triazole is a chemical compound with the molecular formula C7H5N5O2. It is a derivative of 1,2,4-triazole, a five-membered heterocyclic ring containing three nitrogen atoms and one carbon atom. The compound is characterized by the presence of a m-nitrophenyl group, which is a nitro group (-NO2) attached to the meta position of a phenyl ring (C6H5). This chemical has potential applications in various fields, such as pharmaceuticals and agrochemicals, due to its unique structure and reactivity. However, it is essential to handle 5-(m-nitrophenyl)-1H-1,2,4-triazole with caution, as it may possess hazardous properties and require proper safety measures during its synthesis and use.

6219-53-0

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6219-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6219-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,1 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6219-53:
(6*6)+(5*2)+(4*1)+(3*9)+(2*5)+(1*3)=90
90 % 10 = 0
So 6219-53-0 is a valid CAS Registry Number.

6219-53-0Downstream Products

6219-53-0Relevant academic research and scientific papers

A new, high-yield synthesis of 3-aryl-1,2,4-triazoles

Guirado, Antonio,López-Caracena, Libertad,López-Sánchez, José I.,Sandoval, José,Vera, María,Bautista, Delia,Gálvez, Jesús

, p. 8055 - 8060 (2016/11/19)

A convenient new synthetic approach to 3-aryl-1,2,4-triazoles has been developed. Chloralamides were obtained by high yield reactions between benzamides and chloral hydrate. These reacted with a phosphorus pentachloride/phosphorus oxychloride mixture unde

SUBSTITUENT AND COORDINATION EFFECTS IN SINGLET REACTIONS OF 3-DIAZO-3H-1,2,4-TRIAZOLES WITH SUBSTITUTED BENZENES AND NITRO COMPOUNDS

Glinka, J.,Fiscus, D.,Rao, C. B.,Shechter, H.

, p. 3221 - 3224 (2007/10/02)

3-Diazo-3H-1,2,4-triazoles convert to singlet 3H-1,2,4-triazol-3-ylidenes which (1) effect directed electrophilic substitutions of benzenes and (2) coordinate with benzenoid substituents and nitro compounds to give decomposition or rearrangement products.

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